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Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.

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Title: Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.
Authors: Rius R; Centre for Population Genomics, Garvan Institute of Medical Research, UNSW Sydney, Sydney, New South Wales, Australia.; Centre for Population Genomics, Murdoch Children's Research Institute, Melbourne, Victoria, Australia., Blakes AJM; Manchester Centre for Genomic Medicine, Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK., Chen Y; Big Data Institute, University of Oxford, Oxford, UK.; Centre for Human Genetics, University of Oxford, Oxford, UK., De Jonghe J; The Genome Function Laboratory, The Francis Crick Institute, London, UK., Lecoquierre F; Big Data Institute, University of Oxford, Oxford, UK.; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Abnormalities, Rouen, France., Dawes R; Big Data Institute, University of Oxford, Oxford, UK.; Centre for Human Genetics, University of Oxford, Oxford, UK., Cogne B; Nantes Université, CHU de Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Nantes Université, CHU de Nantes, CNRS, INSERM, Génétique médicale, Nantes, France., Kim HC; Big Data Institute, University of Oxford, Oxford, UK.; Centre for Human Genetics, University of Oxford, Oxford, UK., Alvi JR; Department of Pediatric Neurology, University of Child Health Sciences, The Children's Hospital, Lahore, Pakistan., Amblard F; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France., Ansari M; South East Scotland Clinical Genetics Service, NHS lothian, Edinburgh, UK., Arlt A; Institute for Genomic Statistics and Bioinformatics, Medical Faculty, University of Bonn, Bonn, Germany., Austin-Tse C; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Department of Pathology, Harvard Medical School, Boston, MA, USA., Baer S; Department of Neuropediatrics, ERN EpiCare, French Centre de référence des Épilepsies Rares (CréER), Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Institute for Genetics and Molecular and Cellular Biology (IGBMC), University of Strasbourg, CNRS UMR7104, Illkirch, France., Balasubramanian M; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.; Sheffield Clinical Genomics Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK., Balton EV; Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA., Barcia G; Genomic Medecine of Rare Disease, Necker Hospital, Paris, France.; Imagine Institute, Paris, France., Beleza-Meireles A; Clinical Genetics Department, Guy's and St Thomas' NHS Foundation Trust, London, UK., Bernstein JA; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA., Beygo J; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany., Blanc P; Laboratoire SeqOIA, Paris, France., Bramswig NC; Department of Medical Genetics, Centre of Medical Genetics, University and University Hospital Münster, Münster, Germany., Braun F; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany., Buchzik D; Department of Neuropediatrics, Diak Klinikum Landkreis Schwäbisch Hall, Schwäbisch Hall, Germany., Calame DG; Section of Pediatric Neurology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Texas Children's Hospital, Houston, TX, USA., Campbell J; South East Scotland Clinical Genetics Service, NHS lothian, Edinburgh, UK., Coutton C; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France., Cunningham CA; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia., Dargie N; Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA., Depienne C; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany., Dipple KM; Department of Pediatrics, University of Washington, Seattle, WA, USA.; Brotman Baty Institute for Precision Medicine, Seattle, WA, USA., Dieux A; CHU Lille, ULR7364 - RADEME - Maladies Rares du Développement Embryonnaire, Lille, France.; Clinique de Génétique, Hôpital Jeanne de Flandre, CHU de Lille, Lille, France., Dixit A; Clinical Genetics, Nottingham University Hospitals, Nottingham, UK., Dreyer L; Genetic Health WA, Perth, Western Australia, Australia., Du H; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA., El Chehadeh S; Service de Génétique Médicale, Institut de Génétique Médicale D'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Laboratoire de Génétique Médicale, Institut de Génétique Médicale d'Alsace, INSERM UMRS_1112, CRBS, Université de Strasbourg, Strasbourg, France., Field M; Genetics of Learning Disability Service, Hunter Genetics, Waratah, Western Australia, Australia., Ewans LJ; Centre for Clinical Genetics, Sydney Children's Hospitals Network, Sydney, New South Wales, Australia.; Genomics and Inherited Diseases Program, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.; Discipline of Paediatrics and Child Health, School of Clinical Medicine, Faculty of Medicine and Health, University of New South Wales, Sydney, New South Wales, Australia., Geiger V; Genetikum, MVZ genetikum GmbH, Neu-Ulm, Germany., Gibbs RA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA., Glass I; Department of Pediatrics, University of Washington, Seattle, WA, USA.; Brotman Baty Institute for Precision Medicine, Seattle, WA, USA., Grunewald O; U1172-LilNCog-Lille Neuroscience & Cognition, CHU de Lille, Lille, France.; Laboratoire de Genopathies, CHU Lille, Lille, France., Gueguen P; Laboratoire SeqOIA, Paris, France.; Service de Génétique, CHRU de Tours, Tours, France.; Université de Tours, INSERM, Imaging Brain & Neuropsychiatry iBraiN, Tours, France., Haack TB; Institute of Medical Genetics and Applied Genomics, Eberhard Karls University, Tübingen, Germany., Hadj Abdallah H; Genomic Medecine of Rare Disease, Necker Hospital, Paris, France.; Imagine Institute, Paris, France., Harbuz R; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France., Helbig I; The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Epilepsy and Neurodevelopmental Disorders Center (ENDD), Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Division of Neurology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA., Horvath J; Department of Medical Genetics, Centre of Medical Genetics, University and University Hospital Münster, Münster, Germany., Hustinx A; Institute for Genomic Statistics and Bioinformatics, Medical Faculty, University of Bonn, Bonn, Germany., Isidor B; Service de Génétique Médicale, Institut de Génétique Médicale D'Alsace, Centre Hospitalier Universitaire de Nantes, Nantes, France., Jacquemont ML; Service de Génétique, CHRU de Tours, Tours, France.; Université de Tours, INSERM, Imaging Brain & Neuropsychiatry iBraiN, Tours, France.; Centre de Référence Maladies Rares 'Anomalies du Développement et Syndromes Malformatifs', FHU Genomeds, CHRU de Tours, Tours, France., Jamie F; Rare Disease Institute, Division of Genetics and Metabolism and Center for Genetic Medicine Research, Children's National Hospital, Washington, DC, USA., Jeanne M; Service de Génétique, CHRU de Tours, Tours, France.; Université de Tours, INSERM, Imaging Brain & Neuropsychiatry iBraiN, Tours, France.; Centre de Référence Maladies Rares 'Anomalies du Développement et Syndromes Malformatifs', FHU Genomeds, CHRU de Tours, Tours, France.; PRISME division for congenital and Developmental Disorders, Department of Genetics, Hôpital de l'Estran, Avranches, France., Kessler R; Division of Neurology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA., Klinkhammer H; Institute for Genomic Statistics and Bioinformatics, Medical Faculty, University of Bonn, Bonn, Germany.; Institute for Medical Biometry and Statistics, Marburg University, Marburg, Germany., Korenke GC; Department of Neuropediatrics, University Children's Hospital, Klinikum Oldenburg, Oldenburg, Germany., Kotzaeridou U; Department of Pediatrics I, Division of Pediatric Neurology and Metabolic Medicine, Medical Faculty of Heidelberg, Heidelberg, Germany., Krawitz P; Institute for Genomic Statistics and Bioinformatics, Medical Faculty, University of Bonn, Bonn, Germany., Laurie S; Centro Nacional de Análisis Genómico (CNAG), Baldiri Reixac 4, Barcelona, Spain.; Universitat de Barcelona (UB), Barcelona, Spain., Leventer RJ; Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia.; Murdoch Children's Research Institute, Melbourne, Victoria, Australia.; Royal Children's Hospital, Melbourne, Victoria, Australia., Levy RJ; Division of Child Neurology, Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA., Lupski JR; Texas Children's Hospital, Houston, TX, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA., Marijon P; Laboratoire SeqOIA, Paris, France., McGinnis KE; Genetic Health WA, Perth, Western Australia, Australia., Mendez R; Cardiovascular Medicine, Stanford University, Stanford, CA, USA., Messaoud O; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA.; Harvard Medical School, Boston, MA, USA., Nava C; Laboratoire SeqOIA, Paris, France.; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, APHP, Département de Génétique, Hôpital de la Pitié Salpêtrière, Paris, France., Nizard M; Genomic Medecine of Rare Disease, Necker Hospital, Paris, France.; Imagine Institute, Paris, France.; Paris Cité University, Paris, France., O'Donnell-Luria A; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA.; Department of Pediatrics, Harvard Medical School, Boston, MA, USA., O'Leary MC; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA., Olivieri S; Institute of Medical Genetics and Applied Genomics, Eberhard Karls University, Tübingen, Germany., Parida A; Department of Paediatric Neurology, Birmingham Women's and Children's Hospital Foundation Trust, Birmingham, UK., Pehlivan D; Section of Pediatric Neurology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Texas Children's Hospital, Houston, TX, USA., Prentice AJ; The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Division of Neurology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA., Posey JE; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA., Reuter CM; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.; Cardiovascular Medicine, Stanford University, Stanford, CA, USA., Satre V; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France., Schluth-Bolard C; GCS AURAGEN, Lyon, France.; Laboratoire de Diagnostic Génétique, Institut de Génétique Médicale d'Alsace, INSERM UMRS_1112, Université de Strasbourg, Hôpitaux Universitaires de Strasbourg, Strasbourg, France., Smol T; CHU Lille, ULR7364 - RADEME - Maladies Rares du Développement Embryonnaire, Lille, France., Sultan T; Department of Pediatric Neurology, University of Child Health Sciences, The Children's Hospital, Lahore, Pakistan., Taylor J; Department of Radiology, NHS lothian, Edinburgh, UK., Thauvin-Robinet C; Université Bourgogne Europe - CHU Dijon Bourgogne - Inserm U1231 CTM GAD, Centre de Référence des maladies neurogénétiques, Laboratoire de Génomique Médicale, Dijon, France., Thevenon J; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France., Uebergang E; Murdoch Children's Research Institute, Melbourne, Victoria, Australia., Ueberberg S; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany., Vincent-Delorme C; Clinique de Génétique, Hôpital Jeanne de Flandre, CHU de Lille, Lille, France.; Consultation de génétique, CH Arras, Arras, France., Wassmer E; Birmingham Children's Hospital, Birmingham, UK.; Institute of Health and Neurodevelopment, Aston University, Birmingham, UK., Westwood E; NHS Education for Scotland, NHS Scotland, Edinburgh, UK., Wheeler MT; Cardiovascular Medicine, Stanford University, Stanford, CA, USA., Gulec EY; Department of Medical Genetics, Istanbul Medeniyet University Medical School, Istanbul, Turkey.; Medical Genetics Clinic, Istanbul Goztepe Prof Dr Suleyman Yalcin City Hospital, Istanbul, Turkey., Vanderver A; Division of Neurology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA., Vossough A; Department of Radiology, Children's Hospital of Philadelphia, Philadelphia, PA, USA., Sanders SJ; Institute of Developmental and Regenerative Medicine, Department of Paediatrics, University of Oxford, Oxford, UK.; Department of Psychiatry and Behavioral Sciences, UCSF Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, USA., Banka S; Manchester Centre for Genomic Medicine, Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK., Findlay GM; The Genome Function Laboratory, The Francis Crick Institute, London, UK., MacArthur DG; Centre for Population Genomics, Garvan Institute of Medical Research, UNSW Sydney, Sydney, New South Wales, Australia.; Centre for Population Genomics, Murdoch Children's Research Institute, Melbourne, Victoria, Australia., Simons C; Centre for Population Genomics, Garvan Institute of Medical Research, UNSW Sydney, Sydney, New South Wales, Australia. cas.simons@populationgenomics.org.au.; Centre for Population Genomics, Murdoch Children's Research Institute, Melbourne, Victoria, Australia. cas.simons@populationgenomics.org.au., Whiffin N; Big Data Institute, University of Oxford, Oxford, UK. nwhiffin@well.ox.ac.uk.; Centre for Human Genetics, University of Oxford, Oxford, UK. nwhiffin@well.ox.ac.uk.; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA. nwhiffin@well.ox.ac.uk.
Source: Nature genetics [Nat Genet] 2026 Jun; Vol. 58 (6), pp. 1447.
Publication Type: Published Erratum
Journal Info: Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print Cited Medium: Internet ISSN: 1546-1718 (Electronic) Linking ISSN: 10614036 NLM ISO Abbreviation: Nat Genet Subsets: MEDLINE; In Process
Database: MEDLINE Ultimate
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Items – Name: Title
  Label: Title
  Group: Ti
  Data: Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Rius+R%22">Rius R</searchLink>; Centre for Population Genomics, Garvan Institute of Medical Research, UNSW Sydney, Sydney, New South Wales, Australia.; Centre for Population Genomics, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Blakes+AJM%22">Blakes AJM</searchLink>; Manchester Centre for Genomic Medicine, Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Chen+Y%22">Chen Y</searchLink>; Big Data Institute, University of Oxford, Oxford, UK.; Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22De+Jonghe+J%22">De Jonghe J</searchLink>; The Genome Function Laboratory, The Francis Crick Institute, London, UK.<br /><searchLink fieldCode="AU" term="%22Lecoquierre+F%22">Lecoquierre F</searchLink>; Big Data Institute, University of Oxford, Oxford, UK.; Univ Rouen Normandie, Inserm U1245 and CHU Rouen, Department of Genetics and Reference Center for Developmental Abnormalities, Rouen, France.<br /><searchLink fieldCode="AU" term="%22Dawes+R%22">Dawes R</searchLink>; Big Data Institute, University of Oxford, Oxford, UK.; Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Cogne+B%22">Cogne B</searchLink>; Nantes Université, CHU de Nantes, CNRS, INSERM, l'institut du thorax, Nantes, France.; Nantes Université, CHU de Nantes, CNRS, INSERM, Génétique médicale, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Kim+HC%22">Kim HC</searchLink>; Big Data Institute, University of Oxford, Oxford, UK.; Centre for Human Genetics, University of Oxford, Oxford, UK.<br /><searchLink fieldCode="AU" term="%22Alvi+JR%22">Alvi JR</searchLink>; Department of Pediatric Neurology, University of Child Health Sciences, The Children's Hospital, Lahore, Pakistan.<br /><searchLink fieldCode="AU" term="%22Amblard+F%22">Amblard F</searchLink>; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Ansari+M%22">Ansari M</searchLink>; South East Scotland Clinical Genetics Service, NHS lothian, Edinburgh, UK.<br /><searchLink fieldCode="AU" term="%22Arlt+A%22">Arlt A</searchLink>; Institute for Genomic Statistics and Bioinformatics, Medical Faculty, University of Bonn, Bonn, Germany.<br /><searchLink fieldCode="AU" term="%22Austin-Tse+C%22">Austin-Tse C</searchLink>; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Department of Pathology, Harvard Medical School, Boston, MA, USA.<br /><searchLink fieldCode="AU" term="%22Baer+S%22">Baer S</searchLink>; Department of Neuropediatrics, ERN EpiCare, French Centre de référence des Épilepsies Rares (CréER), Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Institute for Genetics and Molecular and Cellular Biology (IGBMC), University of Strasbourg, CNRS UMR7104, Illkirch, France.<br /><searchLink fieldCode="AU" term="%22Balasubramanian+M%22">Balasubramanian M</searchLink>; Division of Clinical Medicine, School of Medicine and Population Health, University of Sheffield, Sheffield, UK.; Sheffield Clinical Genomics Service, Sheffield Children's NHS Foundation Trust, Sheffield, UK.<br /><searchLink fieldCode="AU" term="%22Balton+EV%22">Balton EV</searchLink>; Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA.<br /><searchLink fieldCode="AU" term="%22Barcia+G%22">Barcia G</searchLink>; Genomic Medecine of Rare Disease, Necker Hospital, Paris, France.; Imagine Institute, Paris, France.<br /><searchLink fieldCode="AU" term="%22Beleza-Meireles+A%22">Beleza-Meireles A</searchLink>; Clinical Genetics Department, Guy's and St Thomas' NHS Foundation Trust, London, UK.<br /><searchLink fieldCode="AU" term="%22Bernstein+JA%22">Bernstein JA</searchLink>; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.<br /><searchLink fieldCode="AU" term="%22Beygo+J%22">Beygo J</searchLink>; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.<br /><searchLink fieldCode="AU" term="%22Blanc+P%22">Blanc P</searchLink>; Laboratoire SeqOIA, Paris, France.<br /><searchLink fieldCode="AU" term="%22Bramswig+NC%22">Bramswig NC</searchLink>; Department of Medical Genetics, Centre of Medical Genetics, University and University Hospital Münster, Münster, Germany.<br /><searchLink fieldCode="AU" term="%22Braun+F%22">Braun F</searchLink>; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.<br /><searchLink fieldCode="AU" term="%22Buchzik+D%22">Buchzik D</searchLink>; Department of Neuropediatrics, Diak Klinikum Landkreis Schwäbisch Hall, Schwäbisch Hall, Germany.<br /><searchLink fieldCode="AU" term="%22Calame+DG%22">Calame DG</searchLink>; Section of Pediatric Neurology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Texas Children's Hospital, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Campbell+J%22">Campbell J</searchLink>; South East Scotland Clinical Genetics Service, NHS lothian, Edinburgh, UK.<br /><searchLink fieldCode="AU" term="%22Coutton+C%22">Coutton C</searchLink>; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Cunningham+CA%22">Cunningham CA</searchLink>; Victorian Clinical Genetics Services, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.; Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Dargie+N%22">Dargie N</searchLink>; Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA.<br /><searchLink fieldCode="AU" term="%22Depienne+C%22">Depienne C</searchLink>; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.<br /><searchLink fieldCode="AU" term="%22Dipple+KM%22">Dipple KM</searchLink>; Department of Pediatrics, University of Washington, Seattle, WA, USA.; Brotman Baty Institute for Precision Medicine, Seattle, WA, USA.<br /><searchLink fieldCode="AU" term="%22Dieux+A%22">Dieux A</searchLink>; CHU Lille, ULR7364 - RADEME - Maladies Rares du Développement Embryonnaire, Lille, France.; Clinique de Génétique, Hôpital Jeanne de Flandre, CHU de Lille, Lille, France.<br /><searchLink fieldCode="AU" term="%22Dixit+A%22">Dixit A</searchLink>; Clinical Genetics, Nottingham University Hospitals, Nottingham, UK.<br /><searchLink fieldCode="AU" term="%22Dreyer+L%22">Dreyer L</searchLink>; Genetic Health WA, Perth, Western Australia, Australia.<br /><searchLink fieldCode="AU" term="%22Du+H%22">Du H</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22El+Chehadeh+S%22">El Chehadeh S</searchLink>; Service de Génétique Médicale, Institut de Génétique Médicale D'Alsace, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Laboratoire de Génétique Médicale, Institut de Génétique Médicale d'Alsace, INSERM UMRS_1112, CRBS, Université de Strasbourg, Strasbourg, France.<br /><searchLink fieldCode="AU" term="%22Field+M%22">Field M</searchLink>; Genetics of Learning Disability Service, Hunter Genetics, Waratah, Western Australia, Australia.<br /><searchLink fieldCode="AU" term="%22Ewans+LJ%22">Ewans LJ</searchLink>; Centre for Clinical Genetics, Sydney Children's Hospitals Network, Sydney, New South Wales, Australia.; Genomics and Inherited Diseases Program, Garvan Institute of Medical Research, Darlinghurst, New South Wales, Australia.; Discipline of Paediatrics and Child Health, School of Clinical Medicine, Faculty of Medicine and Health, University of New South Wales, Sydney, New South Wales, Australia.<br /><searchLink fieldCode="AU" term="%22Geiger+V%22">Geiger V</searchLink>; Genetikum, MVZ genetikum GmbH, Neu-Ulm, Germany.<br /><searchLink fieldCode="AU" term="%22Gibbs+RA%22">Gibbs RA</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Glass+I%22">Glass I</searchLink>; Department of Pediatrics, University of Washington, Seattle, WA, USA.; Brotman Baty Institute for Precision Medicine, Seattle, WA, USA.<br /><searchLink fieldCode="AU" term="%22Grunewald+O%22">Grunewald O</searchLink>; U1172-LilNCog-Lille Neuroscience & Cognition, CHU de Lille, Lille, France.; Laboratoire de Genopathies, CHU Lille, Lille, France.<br /><searchLink fieldCode="AU" term="%22Gueguen+P%22">Gueguen P</searchLink>; Laboratoire SeqOIA, Paris, France.; Service de Génétique, CHRU de Tours, Tours, France.; Université de Tours, INSERM, Imaging Brain & Neuropsychiatry iBraiN, Tours, France.<br /><searchLink fieldCode="AU" term="%22Haack+TB%22">Haack TB</searchLink>; Institute of Medical Genetics and Applied Genomics, Eberhard Karls University, Tübingen, Germany.<br /><searchLink fieldCode="AU" term="%22Hadj+Abdallah+H%22">Hadj Abdallah H</searchLink>; Genomic Medecine of Rare Disease, Necker Hospital, Paris, France.; Imagine Institute, Paris, France.<br /><searchLink fieldCode="AU" term="%22Harbuz+R%22">Harbuz R</searchLink>; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Helbig+I%22">Helbig I</searchLink>; The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Epilepsy and Neurodevelopmental Disorders Center (ENDD), Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Division of Neurology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.<br /><searchLink fieldCode="AU" term="%22Horvath+J%22">Horvath J</searchLink>; Department of Medical Genetics, Centre of Medical Genetics, University and University Hospital Münster, Münster, Germany.<br /><searchLink fieldCode="AU" term="%22Hustinx+A%22">Hustinx A</searchLink>; Institute for Genomic Statistics and Bioinformatics, Medical Faculty, University of Bonn, Bonn, Germany.<br /><searchLink fieldCode="AU" term="%22Isidor+B%22">Isidor B</searchLink>; Service de Génétique Médicale, Institut de Génétique Médicale D'Alsace, Centre Hospitalier Universitaire de Nantes, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Jacquemont+ML%22">Jacquemont ML</searchLink>; Service de Génétique, CHRU de Tours, Tours, France.; Université de Tours, INSERM, Imaging Brain & Neuropsychiatry iBraiN, Tours, France.; Centre de Référence Maladies Rares 'Anomalies du Développement et Syndromes Malformatifs', FHU Genomeds, CHRU de Tours, Tours, France.<br /><searchLink fieldCode="AU" term="%22Jamie+F%22">Jamie F</searchLink>; Rare Disease Institute, Division of Genetics and Metabolism and Center for Genetic Medicine Research, Children's National Hospital, Washington, DC, USA.<br /><searchLink fieldCode="AU" term="%22Jeanne+M%22">Jeanne M</searchLink>; Service de Génétique, CHRU de Tours, Tours, France.; Université de Tours, INSERM, Imaging Brain & Neuropsychiatry iBraiN, Tours, France.; Centre de Référence Maladies Rares 'Anomalies du Développement et Syndromes Malformatifs', FHU Genomeds, CHRU de Tours, Tours, France.; PRISME division for congenital and Developmental Disorders, Department of Genetics, Hôpital de l'Estran, Avranches, France.<br /><searchLink fieldCode="AU" term="%22Kessler+R%22">Kessler R</searchLink>; Division of Neurology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.<br /><searchLink fieldCode="AU" term="%22Klinkhammer+H%22">Klinkhammer H</searchLink>; Institute for Genomic Statistics and Bioinformatics, Medical Faculty, University of Bonn, Bonn, Germany.; Institute for Medical Biometry and Statistics, Marburg University, Marburg, Germany.<br /><searchLink fieldCode="AU" term="%22Korenke+GC%22">Korenke GC</searchLink>; Department of Neuropediatrics, University Children's Hospital, Klinikum Oldenburg, Oldenburg, Germany.<br /><searchLink fieldCode="AU" term="%22Kotzaeridou+U%22">Kotzaeridou U</searchLink>; Department of Pediatrics I, Division of Pediatric Neurology and Metabolic Medicine, Medical Faculty of Heidelberg, Heidelberg, Germany.<br /><searchLink fieldCode="AU" term="%22Krawitz+P%22">Krawitz P</searchLink>; Institute for Genomic Statistics and Bioinformatics, Medical Faculty, University of Bonn, Bonn, Germany.<br /><searchLink fieldCode="AU" term="%22Laurie+S%22">Laurie S</searchLink>; Centro Nacional de Análisis Genómico (CNAG), Baldiri Reixac 4, Barcelona, Spain.; Universitat de Barcelona (UB), Barcelona, Spain.<br /><searchLink fieldCode="AU" term="%22Leventer+RJ%22">Leventer RJ</searchLink>; Department of Paediatrics, University of Melbourne, Melbourne, Victoria, Australia.; Murdoch Children's Research Institute, Melbourne, Victoria, Australia.; Royal Children's Hospital, Melbourne, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Levy+RJ%22">Levy RJ</searchLink>; Division of Child Neurology, Department of Neurology and Neurological Sciences, Stanford University, Stanford, CA, USA.<br /><searchLink fieldCode="AU" term="%22Lupski+JR%22">Lupski JR</searchLink>; Texas Children's Hospital, Houston, TX, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Marijon+P%22">Marijon P</searchLink>; Laboratoire SeqOIA, Paris, France.<br /><searchLink fieldCode="AU" term="%22McGinnis+KE%22">McGinnis KE</searchLink>; Genetic Health WA, Perth, Western Australia, Australia.<br /><searchLink fieldCode="AU" term="%22Mendez+R%22">Mendez R</searchLink>; Cardiovascular Medicine, Stanford University, Stanford, CA, USA.<br /><searchLink fieldCode="AU" term="%22Messaoud+O%22">Messaoud O</searchLink>; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA.; Harvard Medical School, Boston, MA, USA.<br /><searchLink fieldCode="AU" term="%22Nava+C%22">Nava C</searchLink>; Laboratoire SeqOIA, Paris, France.; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, APHP, Département de Génétique, Hôpital de la Pitié Salpêtrière, Paris, France.<br /><searchLink fieldCode="AU" term="%22Nizard+M%22">Nizard M</searchLink>; Genomic Medecine of Rare Disease, Necker Hospital, Paris, France.; Imagine Institute, Paris, France.; Paris Cité University, Paris, France.<br /><searchLink fieldCode="AU" term="%22O'Donnell-Luria+A%22">O'Donnell-Luria A</searchLink>; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, USA.; Department of Pediatrics, Harvard Medical School, Boston, MA, USA.<br /><searchLink fieldCode="AU" term="%22O'Leary+MC%22">O'Leary MC</searchLink>; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.<br /><searchLink fieldCode="AU" term="%22Olivieri+S%22">Olivieri S</searchLink>; Institute of Medical Genetics and Applied Genomics, Eberhard Karls University, Tübingen, Germany.<br /><searchLink fieldCode="AU" term="%22Parida+A%22">Parida A</searchLink>; Department of Paediatric Neurology, Birmingham Women's and Children's Hospital Foundation Trust, Birmingham, UK.<br /><searchLink fieldCode="AU" term="%22Pehlivan+D%22">Pehlivan D</searchLink>; Section of Pediatric Neurology, Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.; Texas Children's Hospital, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Prentice+AJ%22">Prentice AJ</searchLink>; The Epilepsy NeuroGenetics Initiative (ENGIN), Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Division of Neurology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.<br /><searchLink fieldCode="AU" term="%22Posey+JE%22">Posey JE</searchLink>; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.<br /><searchLink fieldCode="AU" term="%22Reuter+CM%22">Reuter CM</searchLink>; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, USA.; Cardiovascular Medicine, Stanford University, Stanford, CA, USA.<br /><searchLink fieldCode="AU" term="%22Satre+V%22">Satre V</searchLink>; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Schluth-Bolard+C%22">Schluth-Bolard C</searchLink>; GCS AURAGEN, Lyon, France.; Laboratoire de Diagnostic Génétique, Institut de Génétique Médicale d'Alsace, INSERM UMRS_1112, Université de Strasbourg, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.<br /><searchLink fieldCode="AU" term="%22Smol+T%22">Smol T</searchLink>; CHU Lille, ULR7364 - RADEME - Maladies Rares du Développement Embryonnaire, Lille, France.<br /><searchLink fieldCode="AU" term="%22Sultan+T%22">Sultan T</searchLink>; Department of Pediatric Neurology, University of Child Health Sciences, The Children's Hospital, Lahore, Pakistan.<br /><searchLink fieldCode="AU" term="%22Taylor+J%22">Taylor J</searchLink>; Department of Radiology, NHS lothian, Edinburgh, UK.<br /><searchLink fieldCode="AU" term="%22Thauvin-Robinet+C%22">Thauvin-Robinet C</searchLink>; Université Bourgogne Europe - CHU Dijon Bourgogne - Inserm U1231 CTM GAD, Centre de Référence des maladies neurogénétiques, Laboratoire de Génomique Médicale, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Thevenon+J%22">Thevenon J</searchLink>; Service de Génétique, Génomique et Procréation, CHU Grenoble Alpes, Grenoble, France.; GCS AURAGEN, Lyon, France.; Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France.<br /><searchLink fieldCode="AU" term="%22Uebergang+E%22">Uebergang E</searchLink>; Murdoch Children's Research Institute, Melbourne, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Ueberberg+S%22">Ueberberg S</searchLink>; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.<br /><searchLink fieldCode="AU" term="%22Vincent-Delorme+C%22">Vincent-Delorme C</searchLink>; Clinique de Génétique, Hôpital Jeanne de Flandre, CHU de Lille, Lille, France.; Consultation de génétique, CH Arras, Arras, France.<br /><searchLink fieldCode="AU" term="%22Wassmer+E%22">Wassmer E</searchLink>; Birmingham Children's Hospital, Birmingham, UK.; Institute of Health and Neurodevelopment, Aston University, Birmingham, UK.<br /><searchLink fieldCode="AU" term="%22Westwood+E%22">Westwood E</searchLink>; NHS Education for Scotland, NHS Scotland, Edinburgh, UK.<br /><searchLink fieldCode="AU" term="%22Wheeler+MT%22">Wheeler MT</searchLink>; Cardiovascular Medicine, Stanford University, Stanford, CA, USA.<br /><searchLink fieldCode="AU" term="%22Gulec+EY%22">Gulec EY</searchLink>; Department of Medical Genetics, Istanbul Medeniyet University Medical School, Istanbul, Turkey.; Medical Genetics Clinic, Istanbul Goztepe Prof Dr Suleyman Yalcin City Hospital, Istanbul, Turkey.<br /><searchLink fieldCode="AU" term="%22Vanderver+A%22">Vanderver A</searchLink>; Division of Neurology, Department of Pediatrics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.; Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.<br /><searchLink fieldCode="AU" term="%22Vossough+A%22">Vossough A</searchLink>; Department of Radiology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.<br /><searchLink fieldCode="AU" term="%22Sanders+SJ%22">Sanders SJ</searchLink>; Institute of Developmental and Regenerative Medicine, Department of Paediatrics, University of Oxford, Oxford, UK.; Department of Psychiatry and Behavioral Sciences, UCSF Weill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, USA.<br /><searchLink fieldCode="AU" term="%22Banka+S%22">Banka S</searchLink>; Manchester Centre for Genomic Medicine, Division of Evolution and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.; Manchester Centre for Genomic Medicine, St Mary's Hospital, Manchester University NHS Foundation Trust, Health Innovation Manchester, Manchester, UK.<br /><searchLink fieldCode="AU" term="%22Findlay+GM%22">Findlay GM</searchLink>; The Genome Function Laboratory, The Francis Crick Institute, London, UK.<br /><searchLink fieldCode="AU" term="%22MacArthur+DG%22">MacArthur DG</searchLink>; Centre for Population Genomics, Garvan Institute of Medical Research, UNSW Sydney, Sydney, New South Wales, Australia.; Centre for Population Genomics, Murdoch Children's Research Institute, Melbourne, Victoria, Australia.<br /><searchLink fieldCode="AU" term="%22Simons+C%22">Simons C</searchLink>; Centre for Population Genomics, Garvan Institute of Medical Research, UNSW Sydney, Sydney, New South Wales, Australia. cas.simons@populationgenomics.org.au.; Centre for Population Genomics, Murdoch Children's Research Institute, Melbourne, Victoria, Australia. cas.simons@populationgenomics.org.au.<br /><searchLink fieldCode="AU" term="%22Whiffin+N%22">Whiffin N</searchLink>; Big Data Institute, University of Oxford, Oxford, UK. nwhiffin@well.ox.ac.uk.; Centre for Human Genetics, University of Oxford, Oxford, UK. nwhiffin@well.ox.ac.uk.; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA. nwhiffin@well.ox.ac.uk.
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  Data: <searchLink fieldCode="JN" term="%229216904%22">Nature genetics</searchLink> [Nat Genet] 2026 Jun; Vol. 58 (6), pp. 1447.
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      – TitleFull: Author Correction: Biallelic variants in the noncoding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes.
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          Name:
            NameFull: Smol T
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          Name:
            NameFull: Sultan T
      – PersonEntity:
          Name:
            NameFull: Taylor J
      – PersonEntity:
          Name:
            NameFull: Thauvin-Robinet C
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          Name:
            NameFull: Thevenon J
      – PersonEntity:
          Name:
            NameFull: Uebergang E
      – PersonEntity:
          Name:
            NameFull: Ueberberg S
      – PersonEntity:
          Name:
            NameFull: Vincent-Delorme C
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          Name:
            NameFull: Wassmer E
      – PersonEntity:
          Name:
            NameFull: Westwood E
      – PersonEntity:
          Name:
            NameFull: Wheeler MT
      – PersonEntity:
          Name:
            NameFull: Gulec EY
      – PersonEntity:
          Name:
            NameFull: Vanderver A
      – PersonEntity:
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            NameFull: Vossough A
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          Name:
            NameFull: Sanders SJ
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            NameFull: Banka S
      – PersonEntity:
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            NameFull: Findlay GM
      – PersonEntity:
          Name:
            NameFull: MacArthur DG
      – PersonEntity:
          Name:
            NameFull: Simons C
      – PersonEntity:
          Name:
            NameFull: Whiffin N
    IsPartOfRelationships:
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          Dates:
            – D: 01
              M: 06
              Text: 2026 Jun
              Type: published
              Y: 2026
          Identifiers:
            – Type: issn-electronic
              Value: 1546-1718
          Numbering:
            – Type: volume
              Value: 58
            – Type: issue
              Value: 6
          Titles:
            – TitleFull: Nature genetics
              Type: main
ResultId 1