View in EDS

Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.

Saved in:
Bibliographic Details
Title: Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.
Authors: Engel C; Université de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France. cengel@chu-besancon.fr.; Université de Bourgogne, INSERM UMR1231 GAD 'Génétique des Anomalies du Développement', Dijon, France. cengel@chu-besancon.fr., Rendek M; Université de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France., Assoumani J; Université de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France., Argilli E; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA., Ariani F; Medical Genetics, University of Siena, Siena, Italy.; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy.; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy., Avice-Denizet AL; Université de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France., Bijlsma EK; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands., Blanc P; Laboratoire Seqoia, Paris, France., Bruno LP; Medical Genetics, University of Siena, Siena, Italy.; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy.; Department of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy., Callewaert B; Reference centre for Mendelian connective tissue disorders-UZ Gent, Ghent University Hospital-UZ Gent, Gent, Belgium., Capra V; Genomics and Clinical Genetics, IRCCS Istituto Giannina Gaslini, Genoa, Italy., Carullo M; Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Roma, Italy., Chesneau B; Service de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France., Coppens S; Center for Medical Genetics, Hôpital Erasme, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium., Curry C; Genetic Medicine, University of California, San Francisco/Fresno, Fresno, CA, USA., Dale B; Genetics and Metabolics Clinic, McMaster Children's Hospital, Hamilton, ON, Canada., Dahlen E; Université de Franche-Comté, CHU Besançon, Oncobiologie Génétique Bioinformatique, FHU-TRANSLAD et Institut GIMI, Besançon, France., Delahaye-Duriez A; UF médecine génomique et génétique clinique, Hôpital Jean Verdier, Hôpitaux Universitaires de Paris Seine Saint Denis, AP-HP, Bondy, France.; UFR de Santé Médecine et Biologie humaine, Université Sorbonne Paris Nord, Bobigny, France.; NeuroDiderot UMR 1141, Inserm, Université de Paris, Paris, France., Denommé-Pichon AS; Université de Bourgogne, INSERM UMR1231 GAD 'Génétique des Anomalies du Développement', Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France., Demeer B; Service de Génétique Clinique et Oncogénétique, CHU Amiens-Picardie, Amiens, France., Dvořáková L; Department of Biology and Medical Genetics, Charles University-2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic., Fischer J; Institute for Clinical Genetics, University Hospital Carl Gustav Carus at TUD Dresden University of Technology, Dresden, Germany., Geneviève D; Université Montpellier, Centre de référence anomalies du développement et syndromes malformatifs, Génétique Clinique, CHU Montpellier, Montpellier, France., Giacomini T; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Child Neuropsychiatry Unit, IRCCS G. Gaslini Institute, Genoa, Italy., Handrup MM; Center for Rare Diseases, Pediatric and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark., Heron D; Département de génétique médicale, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, Paris, France., Hüning I; Institute of Human Genetics, University Hospital Schleswig-Holstein, Lübeck, Germany., Iacomino M; Medical Genetics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy., Isidor B; Service de génétique médicale, Unité de génétique clinique, CHU Hôtel Dieu, 1 place Alexis Ricordeau, Nantes, France., Keren B; Département de génétique médicale, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, Paris, France., Kmoch S; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University in Prague, Prague, Czech Republic., Koolen DA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Kübler A; Institute for Clinical Genetics, University Hospital Carl Gustav Carus at TUD Dresden University of Technology, Dresden, Germany., Laštůvková J; Department of Medical Genetics, Masaryk Hospital in Ústí nad Labem, Regional Health Corporation, Ústí nad Labem, Czech Republic., Le C; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA., Levy J; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France., Rizzo CL; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy., Maitz S; Service of Medical Genetics, Oncologic Institute of Southern Switzerland, EOC, Switzerland, Switzerland., Marlin S; Centre de référence « Surdités Génétiques », Service de Médecine génomique des Maladies rares, Hôpital Necker, Assistance Publique-Hôpitaux de Paris, Paris, France.; Institut Imagine, Paris, France., Mignot C; Département de génétique médicale, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, Paris, France., Mirzaa G; Department of Pediatrics, University of Washington, Seattle, WA, USA.; Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA, USA.; Brotman Baty Institute for Precision Medicine, Seattle, WA, USA., Nagel I; Institute of Human Genetics, University Hospital Schleswig-Holstein, Kiel, Germany., Neuens S; Department of Genetics, Hôpital Universitaire des Enfants Reine Fabiola, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium., Nosková L; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University in Prague, Prague, Czech Republic., Pao E; Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA, USA., Pecková A; Department of Medical Genetics, Masaryk Hospital in Ústí nad Labem, Regional Health Corporation, Ústí nad Labem, Czech Republic., Plaisancie J; Service de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France., Porrmann J; Institute for Clinical Genetics, University Hospital Carl Gustav Carus at TUD Dresden University of Technology, Dresden, Germany., Privitera F; Department of Neurobiology and Molecular Medicine, IRCCS Fondazione Stella Maris, Pisa, Italy., Reis A; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.; Centre for Rare Diseases Erlangen (ZSEER), Erlangen, Germany., Renieri A; Medical Genetics, University of Siena, Siena, Italy.; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy., Rio M; Necker Hospital, APHP, Reference Center for Intellectual Disability, Genetics Department, Institut Imagine, University of Paris, Paris, France., Rippert A; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA., Ryba L; Department of Biology and Medical Genetics, Charles University-2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic., Scala M; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Medical Genetics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy., Schieving JH; Radboud University Medical Center, Department of Neurology, Nijmegen, The Netherlands., Sherr EH; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA., Shuen A; Department of Pediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON, Canada., Sidlow R; Department of Medical Genetics and Metabolism, Valley Children's Hospital, Madera, CA, USA., Smol T; Institut de Génétique Médicale, CHU Lille, Avenue Oscar Lambret, Lille, France., Soblet J; Department of Genetics, Hôpital Universitaire des Enfants Reine Fabiola, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.; Interuniversitary Institute of Bioinformatics in Brussels, Université Libre de Bruxelles, Brussels, Belgium., Striano P; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy., Suri M; Nottingham Clinical Genetics Service, Nottingham University Hospitals NHS Trust, City Hospital Campus, Nottingham, UK., Syryn H; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Department of biomolecular medicine, Ghent university, Ghent, Belgium., Tran Mau-Them F; Université de Bourgogne, INSERM UMR1231 GAD 'Génétique des Anomalies du Développement', Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France., Travessa AM; Department of Medical Genetics, Hospital de Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Lisbon, Portugal.; Institute of Histology and Developmental Biology, Faculty of Medicine, University of Lisbon, Lisbon, Portugal., Van Gils J; Department of Medical Genetics, University Hospital of Bordeaux and INSERM U1211, University of Bordeaux, Bordeaux, France., Vasileiou G; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.; Centre for Rare Diseases Erlangen (ZSEER), Erlangen, Germany., Verseput JJA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands., Vilain C; Department of Genetics, Hôpital Universitaire des Enfants Reine Fabiola, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium., Vincent-Delorme C; CHU Lille, Clinique de Génétique, Lille, France., Vyhnálková E; Department of Biology and Medical Genetics, Charles University-2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic., Wakeling EL; North East Thames Regional Genetic Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK., Zacher P; Epilepsy Center Kleinwachau, Radeberg, Germany., Zara F; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Medical Genetics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy., Kuentz P; Université de Bourgogne, INSERM UMR1231 GAD 'Génétique des Anomalies du Développement', Dijon, France.; Université de Franche-Comté, CHU Besançon, Oncobiologie Génétique Bioinformatique, FHU-TRANSLAD et Institut GIMI, Besançon, France., Piard J; Université de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France. jpiard@chu-besancon.fr.; Université de Bourgogne, INSERM UMR1231 GAD 'Génétique des Anomalies du Développement', Dijon, France. jpiard@chu-besancon.fr.
Source: European journal of human genetics : EJHG [Eur J Hum Genet] 2026 Apr 02. Date of Electronic Publication: 2026 Apr 02.
Publication Type: Published Erratum
Journal Info: Publisher: Nature Publishing Group Country of Publication: England NLM ID: 9302235 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5438 (Electronic) Linking ISSN: 10184813 NLM ISO Abbreviation: Eur J Hum Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
FullText Text:
  Availability: 0
Header DbId: mdl
DbLabel: MEDLINE Ultimate
An: 41927804
AccessLevel: 2
PubTypeId: unknown
PreciseRelevancyScore: 0
IllustrationInfo
Items – Name: Title
  Label: Title
  Group: Ti
  Data: Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AU" term="%22Engel+C%22">Engel C</searchLink>; Université de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France. cengel@chu-besancon.fr.; Université de Bourgogne, INSERM UMR1231 GAD 'Génétique des Anomalies du Développement', Dijon, France. cengel@chu-besancon.fr.<br /><searchLink fieldCode="AU" term="%22Rendek+M%22">Rendek M</searchLink>; Université de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France.<br /><searchLink fieldCode="AU" term="%22Assoumani+J%22">Assoumani J</searchLink>; Université de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France.<br /><searchLink fieldCode="AU" term="%22Argilli+E%22">Argilli E</searchLink>; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA.<br /><searchLink fieldCode="AU" term="%22Ariani+F%22">Ariani F</searchLink>; Medical Genetics, University of Siena, Siena, Italy.; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy.; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.<br /><searchLink fieldCode="AU" term="%22Avice-Denizet+AL%22">Avice-Denizet AL</searchLink>; Université de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France.<br /><searchLink fieldCode="AU" term="%22Bijlsma+EK%22">Bijlsma EK</searchLink>; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Blanc+P%22">Blanc P</searchLink>; Laboratoire Seqoia, Paris, France.<br /><searchLink fieldCode="AU" term="%22Bruno+LP%22">Bruno LP</searchLink>; Medical Genetics, University of Siena, Siena, Italy.; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy.; Department of Medicine and Surgery, University of Milan-Bicocca, Monza, Italy.<br /><searchLink fieldCode="AU" term="%22Callewaert+B%22">Callewaert B</searchLink>; Reference centre for Mendelian connective tissue disorders-UZ Gent, Ghent University Hospital-UZ Gent, Gent, Belgium.<br /><searchLink fieldCode="AU" term="%22Capra+V%22">Capra V</searchLink>; Genomics and Clinical Genetics, IRCCS Istituto Giannina Gaslini, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Carullo+M%22">Carullo M</searchLink>; Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Roma, Italy.<br /><searchLink fieldCode="AU" term="%22Chesneau+B%22">Chesneau B</searchLink>; Service de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.<br /><searchLink fieldCode="AU" term="%22Coppens+S%22">Coppens S</searchLink>; Center for Medical Genetics, Hôpital Erasme, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.<br /><searchLink fieldCode="AU" term="%22Curry+C%22">Curry C</searchLink>; Genetic Medicine, University of California, San Francisco/Fresno, Fresno, CA, USA.<br /><searchLink fieldCode="AU" term="%22Dale+B%22">Dale B</searchLink>; Genetics and Metabolics Clinic, McMaster Children's Hospital, Hamilton, ON, Canada.<br /><searchLink fieldCode="AU" term="%22Dahlen+E%22">Dahlen E</searchLink>; Université de Franche-Comté, CHU Besançon, Oncobiologie Génétique Bioinformatique, FHU-TRANSLAD et Institut GIMI, Besançon, France.<br /><searchLink fieldCode="AU" term="%22Delahaye-Duriez+A%22">Delahaye-Duriez A</searchLink>; UF médecine génomique et génétique clinique, Hôpital Jean Verdier, Hôpitaux Universitaires de Paris Seine Saint Denis, AP-HP, Bondy, France.; UFR de Santé Médecine et Biologie humaine, Université Sorbonne Paris Nord, Bobigny, France.; NeuroDiderot UMR 1141, Inserm, Université de Paris, Paris, France.<br /><searchLink fieldCode="AU" term="%22Denommé-Pichon+AS%22">Denommé-Pichon AS</searchLink>; Université de Bourgogne, INSERM UMR1231 GAD 'Génétique des Anomalies du Développement', Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Demeer+B%22">Demeer B</searchLink>; Service de Génétique Clinique et Oncogénétique, CHU Amiens-Picardie, Amiens, France.<br /><searchLink fieldCode="AU" term="%22Dvořáková+L%22">Dvořáková L</searchLink>; Department of Biology and Medical Genetics, Charles University-2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.<br /><searchLink fieldCode="AU" term="%22Fischer+J%22">Fischer J</searchLink>; Institute for Clinical Genetics, University Hospital Carl Gustav Carus at TUD Dresden University of Technology, Dresden, Germany.<br /><searchLink fieldCode="AU" term="%22Geneviève+D%22">Geneviève D</searchLink>; Université Montpellier, Centre de référence anomalies du développement et syndromes malformatifs, Génétique Clinique, CHU Montpellier, Montpellier, France.<br /><searchLink fieldCode="AU" term="%22Giacomini+T%22">Giacomini T</searchLink>; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Child Neuropsychiatry Unit, IRCCS G. Gaslini Institute, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Handrup+MM%22">Handrup MM</searchLink>; Center for Rare Diseases, Pediatric and Adolescent Medicine, Aarhus University Hospital, Aarhus, Denmark.<br /><searchLink fieldCode="AU" term="%22Heron+D%22">Heron D</searchLink>; Département de génétique médicale, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Hüning+I%22">Hüning I</searchLink>; Institute of Human Genetics, University Hospital Schleswig-Holstein, Lübeck, Germany.<br /><searchLink fieldCode="AU" term="%22Iacomino+M%22">Iacomino M</searchLink>; Medical Genetics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Isidor+B%22">Isidor B</searchLink>; Service de génétique médicale, Unité de génétique clinique, CHU Hôtel Dieu, 1 place Alexis Ricordeau, Nantes, France.<br /><searchLink fieldCode="AU" term="%22Keren+B%22">Keren B</searchLink>; Département de génétique médicale, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Kmoch+S%22">Kmoch S</searchLink>; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.<br /><searchLink fieldCode="AU" term="%22Koolen+DA%22">Koolen DA</searchLink>; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Kübler+A%22">Kübler A</searchLink>; Institute for Clinical Genetics, University Hospital Carl Gustav Carus at TUD Dresden University of Technology, Dresden, Germany.<br /><searchLink fieldCode="AU" term="%22Laštůvková+J%22">Laštůvková J</searchLink>; Department of Medical Genetics, Masaryk Hospital in Ústí nad Labem, Regional Health Corporation, Ústí nad Labem, Czech Republic.<br /><searchLink fieldCode="AU" term="%22Le+C%22">Le C</searchLink>; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA.<br /><searchLink fieldCode="AU" term="%22Levy+J%22">Levy J</searchLink>; Genetics Department, AP-HP, Robert-Debré University Hospital, Paris, France.<br /><searchLink fieldCode="AU" term="%22Rizzo+CL%22">Rizzo CL</searchLink>; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.<br /><searchLink fieldCode="AU" term="%22Maitz+S%22">Maitz S</searchLink>; Service of Medical Genetics, Oncologic Institute of Southern Switzerland, EOC, Switzerland, Switzerland.<br /><searchLink fieldCode="AU" term="%22Marlin+S%22">Marlin S</searchLink>; Centre de référence « Surdités Génétiques », Service de Médecine génomique des Maladies rares, Hôpital Necker, Assistance Publique-Hôpitaux de Paris, Paris, France.; Institut Imagine, Paris, France.<br /><searchLink fieldCode="AU" term="%22Mignot+C%22">Mignot C</searchLink>; Département de génétique médicale, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, Paris, France.<br /><searchLink fieldCode="AU" term="%22Mirzaa+G%22">Mirzaa G</searchLink>; Department of Pediatrics, University of Washington, Seattle, WA, USA.; Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA, USA.; Brotman Baty Institute for Precision Medicine, Seattle, WA, USA.<br /><searchLink fieldCode="AU" term="%22Nagel+I%22">Nagel I</searchLink>; Institute of Human Genetics, University Hospital Schleswig-Holstein, Kiel, Germany.<br /><searchLink fieldCode="AU" term="%22Neuens+S%22">Neuens S</searchLink>; Department of Genetics, Hôpital Universitaire des Enfants Reine Fabiola, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.<br /><searchLink fieldCode="AU" term="%22Nosková+L%22">Nosková L</searchLink>; Research Unit for Rare Diseases, Department of Pediatrics and Inherited Metabolic Disorders, 1st Faculty of Medicine, Charles University in Prague, Prague, Czech Republic.<br /><searchLink fieldCode="AU" term="%22Pao+E%22">Pao E</searchLink>; Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA, USA.<br /><searchLink fieldCode="AU" term="%22Pecková+A%22">Pecková A</searchLink>; Department of Medical Genetics, Masaryk Hospital in Ústí nad Labem, Regional Health Corporation, Ústí nad Labem, Czech Republic.<br /><searchLink fieldCode="AU" term="%22Plaisancie+J%22">Plaisancie J</searchLink>; Service de Génétique Médicale, Hôpital Purpan, CHU de Toulouse, Toulouse, France.<br /><searchLink fieldCode="AU" term="%22Porrmann+J%22">Porrmann J</searchLink>; Institute for Clinical Genetics, University Hospital Carl Gustav Carus at TUD Dresden University of Technology, Dresden, Germany.<br /><searchLink fieldCode="AU" term="%22Privitera+F%22">Privitera F</searchLink>; Department of Neurobiology and Molecular Medicine, IRCCS Fondazione Stella Maris, Pisa, Italy.<br /><searchLink fieldCode="AU" term="%22Reis+A%22">Reis A</searchLink>; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.; Centre for Rare Diseases Erlangen (ZSEER), Erlangen, Germany.<br /><searchLink fieldCode="AU" term="%22Renieri+A%22">Renieri A</searchLink>; Medical Genetics, University of Siena, Siena, Italy.; Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Italy.<br /><searchLink fieldCode="AU" term="%22Rio+M%22">Rio M</searchLink>; Necker Hospital, APHP, Reference Center for Intellectual Disability, Genetics Department, Institut Imagine, University of Paris, Paris, France.<br /><searchLink fieldCode="AU" term="%22Rippert+A%22">Rippert A</searchLink>; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.<br /><searchLink fieldCode="AU" term="%22Ryba+L%22">Ryba L</searchLink>; Department of Biology and Medical Genetics, Charles University-2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.<br /><searchLink fieldCode="AU" term="%22Scala+M%22">Scala M</searchLink>; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Medical Genetics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Schieving+JH%22">Schieving JH</searchLink>; Radboud University Medical Center, Department of Neurology, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Sherr+EH%22">Sherr EH</searchLink>; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA.<br /><searchLink fieldCode="AU" term="%22Shuen+A%22">Shuen A</searchLink>; Department of Pediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON, Canada.<br /><searchLink fieldCode="AU" term="%22Sidlow+R%22">Sidlow R</searchLink>; Department of Medical Genetics and Metabolism, Valley Children's Hospital, Madera, CA, USA.<br /><searchLink fieldCode="AU" term="%22Smol+T%22">Smol T</searchLink>; Institut de Génétique Médicale, CHU Lille, Avenue Oscar Lambret, Lille, France.<br /><searchLink fieldCode="AU" term="%22Soblet+J%22">Soblet J</searchLink>; Department of Genetics, Hôpital Universitaire des Enfants Reine Fabiola, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.; Interuniversitary Institute of Bioinformatics in Brussels, Université Libre de Bruxelles, Brussels, Belgium.<br /><searchLink fieldCode="AU" term="%22Striano+P%22">Striano P</searchLink>; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy.<br /><searchLink fieldCode="AU" term="%22Suri+M%22">Suri M</searchLink>; Nottingham Clinical Genetics Service, Nottingham University Hospitals NHS Trust, City Hospital Campus, Nottingham, UK.<br /><searchLink fieldCode="AU" term="%22Syryn+H%22">Syryn H</searchLink>; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.; Department of biomolecular medicine, Ghent university, Ghent, Belgium.<br /><searchLink fieldCode="AU" term="%22Tran+Mau-Them+F%22">Tran Mau-Them F</searchLink>; Université de Bourgogne, INSERM UMR1231 GAD 'Génétique des Anomalies du Développement', Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic Génomique des Maladies Rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.<br /><searchLink fieldCode="AU" term="%22Travessa+AM%22">Travessa AM</searchLink>; Department of Medical Genetics, Hospital de Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Lisbon, Portugal.; Institute of Histology and Developmental Biology, Faculty of Medicine, University of Lisbon, Lisbon, Portugal.<br /><searchLink fieldCode="AU" term="%22Van+Gils+J%22">Van Gils J</searchLink>; Department of Medical Genetics, University Hospital of Bordeaux and INSERM U1211, University of Bordeaux, Bordeaux, France.<br /><searchLink fieldCode="AU" term="%22Vasileiou+G%22">Vasileiou G</searchLink>; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany.; Centre for Rare Diseases Erlangen (ZSEER), Erlangen, Germany.<br /><searchLink fieldCode="AU" term="%22Verseput+JJA%22">Verseput JJA</searchLink>; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.<br /><searchLink fieldCode="AU" term="%22Vilain+C%22">Vilain C</searchLink>; Department of Genetics, Hôpital Universitaire des Enfants Reine Fabiola, Hôpital Universitaire de Bruxelles, Université Libre de Bruxelles, Brussels, Belgium.<br /><searchLink fieldCode="AU" term="%22Vincent-Delorme+C%22">Vincent-Delorme C</searchLink>; CHU Lille, Clinique de Génétique, Lille, France.<br /><searchLink fieldCode="AU" term="%22Vyhnálková+E%22">Vyhnálková E</searchLink>; Department of Biology and Medical Genetics, Charles University-2nd Faculty of Medicine and University Hospital Motol, Prague, Czech Republic.<br /><searchLink fieldCode="AU" term="%22Wakeling+EL%22">Wakeling EL</searchLink>; North East Thames Regional Genetic Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK.<br /><searchLink fieldCode="AU" term="%22Zacher+P%22">Zacher P</searchLink>; Epilepsy Center Kleinwachau, Radeberg, Germany.<br /><searchLink fieldCode="AU" term="%22Zara+F%22">Zara F</searchLink>; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.; Medical Genetics Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.<br /><searchLink fieldCode="AU" term="%22Kuentz+P%22">Kuentz P</searchLink>; Université de Bourgogne, INSERM UMR1231 GAD 'Génétique des Anomalies du Développement', Dijon, France.; Université de Franche-Comté, CHU Besançon, Oncobiologie Génétique Bioinformatique, FHU-TRANSLAD et Institut GIMI, Besançon, France.<br /><searchLink fieldCode="AU" term="%22Piard+J%22">Piard J</searchLink>; Université de Franche-Comté, Centre de Génétique Humaine, CHU Besançon, Besançon, France. jpiard@chu-besancon.fr.; Université de Bourgogne, INSERM UMR1231 GAD 'Génétique des Anomalies du Développement', Dijon, France. jpiard@chu-besancon.fr.
– Name: TitleSource
  Label: Source
  Group: Src
  Data: <searchLink fieldCode="JN" term="%229302235%22">European journal of human genetics : EJHG</searchLink> [Eur J Hum Genet] 2026 Apr 02. <i>Date of Electronic Publication: </i>2026 Apr 02.
– Name: TypePub
  Label: Publication Type
  Group: TypPub
  Data: Published Erratum
– Name: TitleSource
  Label: Journal Info
  Group: Src
  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Publishing+Group%22">Nature Publishing Group </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9302235 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1476-5438 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210184813%22">10184813 </searchLink><i>NLM ISO Abbreviation: </i>Eur J Hum Genet <i>Subsets: </i>MEDLINE
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=mdl&AN=41927804
RecordInfo BibRecord:
  BibEntity:
    Identifiers:
      – Type: doi
        Value: 10.1038/s41431-026-02087-w
    Languages:
      – Code: eng
        Text: English
    Titles:
      – TitleFull: Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization.
        Type: main
  BibRelationships:
    HasContributorRelationships:
      – PersonEntity:
          Name:
            NameFull: Engel C
      – PersonEntity:
          Name:
            NameFull: Rendek M
      – PersonEntity:
          Name:
            NameFull: Assoumani J
      – PersonEntity:
          Name:
            NameFull: Argilli E
      – PersonEntity:
          Name:
            NameFull: Ariani F
      – PersonEntity:
          Name:
            NameFull: Avice-Denizet AL
      – PersonEntity:
          Name:
            NameFull: Bijlsma EK
      – PersonEntity:
          Name:
            NameFull: Blanc P
      – PersonEntity:
          Name:
            NameFull: Bruno LP
      – PersonEntity:
          Name:
            NameFull: Callewaert B
      – PersonEntity:
          Name:
            NameFull: Capra V
      – PersonEntity:
          Name:
            NameFull: Carullo M
      – PersonEntity:
          Name:
            NameFull: Chesneau B
      – PersonEntity:
          Name:
            NameFull: Coppens S
      – PersonEntity:
          Name:
            NameFull: Curry C
      – PersonEntity:
          Name:
            NameFull: Dale B
      – PersonEntity:
          Name:
            NameFull: Dahlen E
      – PersonEntity:
          Name:
            NameFull: Delahaye-Duriez A
      – PersonEntity:
          Name:
            NameFull: Denommé-Pichon AS
      – PersonEntity:
          Name:
            NameFull: Demeer B
      – PersonEntity:
          Name:
            NameFull: Dvořáková L
      – PersonEntity:
          Name:
            NameFull: Fischer J
      – PersonEntity:
          Name:
            NameFull: Geneviève D
      – PersonEntity:
          Name:
            NameFull: Giacomini T
      – PersonEntity:
          Name:
            NameFull: Handrup MM
      – PersonEntity:
          Name:
            NameFull: Heron D
      – PersonEntity:
          Name:
            NameFull: Hüning I
      – PersonEntity:
          Name:
            NameFull: Iacomino M
      – PersonEntity:
          Name:
            NameFull: Isidor B
      – PersonEntity:
          Name:
            NameFull: Keren B
      – PersonEntity:
          Name:
            NameFull: Kmoch S
      – PersonEntity:
          Name:
            NameFull: Koolen DA
      – PersonEntity:
          Name:
            NameFull: Kübler A
      – PersonEntity:
          Name:
            NameFull: Laštůvková J
      – PersonEntity:
          Name:
            NameFull: Le C
      – PersonEntity:
          Name:
            NameFull: Levy J
      – PersonEntity:
          Name:
            NameFull: Rizzo CL
      – PersonEntity:
          Name:
            NameFull: Maitz S
      – PersonEntity:
          Name:
            NameFull: Marlin S
      – PersonEntity:
          Name:
            NameFull: Mignot C
      – PersonEntity:
          Name:
            NameFull: Mirzaa G
      – PersonEntity:
          Name:
            NameFull: Nagel I
      – PersonEntity:
          Name:
            NameFull: Neuens S
      – PersonEntity:
          Name:
            NameFull: Nosková L
      – PersonEntity:
          Name:
            NameFull: Pao E
      – PersonEntity:
          Name:
            NameFull: Pecková A
      – PersonEntity:
          Name:
            NameFull: Plaisancie J
      – PersonEntity:
          Name:
            NameFull: Porrmann J
      – PersonEntity:
          Name:
            NameFull: Privitera F
      – PersonEntity:
          Name:
            NameFull: Reis A
      – PersonEntity:
          Name:
            NameFull: Renieri A
      – PersonEntity:
          Name:
            NameFull: Rio M
      – PersonEntity:
          Name:
            NameFull: Rippert A
      – PersonEntity:
          Name:
            NameFull: Ryba L
      – PersonEntity:
          Name:
            NameFull: Scala M
      – PersonEntity:
          Name:
            NameFull: Schieving JH
      – PersonEntity:
          Name:
            NameFull: Sherr EH
      – PersonEntity:
          Name:
            NameFull: Shuen A
      – PersonEntity:
          Name:
            NameFull: Sidlow R
      – PersonEntity:
          Name:
            NameFull: Smol T
      – PersonEntity:
          Name:
            NameFull: Soblet J
      – PersonEntity:
          Name:
            NameFull: Striano P
      – PersonEntity:
          Name:
            NameFull: Suri M
      – PersonEntity:
          Name:
            NameFull: Syryn H
      – PersonEntity:
          Name:
            NameFull: Tran Mau-Them F
      – PersonEntity:
          Name:
            NameFull: Travessa AM
      – PersonEntity:
          Name:
            NameFull: Van Gils J
      – PersonEntity:
          Name:
            NameFull: Vasileiou G
      – PersonEntity:
          Name:
            NameFull: Verseput JJA
      – PersonEntity:
          Name:
            NameFull: Vilain C
      – PersonEntity:
          Name:
            NameFull: Vincent-Delorme C
      – PersonEntity:
          Name:
            NameFull: Vyhnálková E
      – PersonEntity:
          Name:
            NameFull: Wakeling EL
      – PersonEntity:
          Name:
            NameFull: Zacher P
      – PersonEntity:
          Name:
            NameFull: Zara F
      – PersonEntity:
          Name:
            NameFull: Kuentz P
      – PersonEntity:
          Name:
            NameFull: Piard J
    IsPartOfRelationships:
      – BibEntity:
          Dates:
            – D: 02
              M: 04
              Text: 2026 Apr 02
              Type: published
              Y: 2026
          Identifiers:
            – Type: issn-electronic
              Value: 1476-5438
          Titles:
            – TitleFull: European journal of human genetics : EJHG
              Type: main
ResultId 1