Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
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| Title: | Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language. |
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| Authors: | Snijders Blok L; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands., Rousseau J; CHU Sainte-Justine Research Center, Montreal, QC H3T 1C5, Canada., Twist J; National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA., Ehresmann S; CHU Sainte-Justine Research Center, Montreal, QC H3T 1C5, Canada., Takaku M; National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA., Venselaar H; Centre for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands., Rodan LH; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA 02115, USA., Nowak CB; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA 02115, USA., Douglas J; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA 02115, USA., Swoboda KJ; Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02114, USA., Steeves MA; Department of Medical Genetics, Massachusetts General Hospital, Boston, MA 02114, USA., Sahai I; Department of Medical Genetics, Massachusetts General Hospital, Boston, MA 02114, USA., Stumpel CTRM; Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands., Stegmann APA; Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands., Wheeler P; Nemours Childrens Clinic, Orlando, FL 32827, USA., Willing M; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA., Fiala E; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO 63110, USA., Kochhar A; Valley Children's Hospital, Madera, CA 93636, USA., Gibson WT; British Columbia Children's Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada.; Department of Medical Genetics, University of British Columbia, Vancouver, BC V6H 3N1, Canada., Cohen ASA; British Columbia Children's Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada.; Department of Medical Genetics, University of British Columbia, Vancouver, BC V6H 3N1, Canada., Agbahovbe R; British Columbia Children's Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada.; Department of Medical Genetics, University of British Columbia, Vancouver, BC V6H 3N1, Canada., Innes AM; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada., Au PYB; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada., Rankin J; Department of Clinical Genetics, Royal Devon and Exeter NHS Foundation Trust (Heavitree), Exeter, EX2 5DW, UK., Anderson IJ; Division of Genetics, Department of Medicine, University of Tennessee Medical Center, Knoxville, TN 37920, USA., Skinner SA; Greenwood Genetic Center, Greenwood, SC 29646, USA., Louie RJ; Greenwood Genetic Center, Greenwood, SC 29646, USA., Warren HE; Greenwood Genetic Center, Greenwood, SC 29646, USA., Afenjar A; GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris ; Department of Medical Genetics and Centre de Référence Malformations et maladies congénitales du cervelet et déficiences intellectuelles de causes rares, Armand Trousseau Hospital, GHUEP, AP-HP, Paris, 75012, France., Keren B; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France.; Groupe de Recherche Clinique (GRC) 'déficience intellectuelle et autisme' UPMC, Paris, 75005, France., Nava C; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France.; Groupe de Recherche Clinique (GRC) 'déficience intellectuelle et autisme' UPMC, Paris, 75005, France.; INSERM, U 1127, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM, Sorbonne Universités, UPMC Univ Paris 06 UMR S 1127, 75013, Paris, France., Buratti J; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France., Isapof A; GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department Child Neurology and Reference Center for Neuromuscular Diseases 'Nord/Est/Ile-de-France', FILNEMUS, Armand Trousseau Hospital, GHUEP, AP-HP, Paris, 75012, France., Rodriguez D; GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department of Child Neurology and National Reference Center for Neurogenetic Disorders, Armand Trousseau Hospital, GHUEP, AP-HP, INSERM U1141, 75012, Paris, France., Lewandowski R; Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA 23298, USA., Propst J; Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA 23298, USA., van Essen T; Clinical Genetics Department, University Medical Center Groningen, Groningen, 9700RB, The Netherlands., Choi M; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea., Lee S; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea., Chae JH; Department of Pediatrics, Seoul National University College of Medicine, Seoul National University Children's Hospital, Seoul, 08826, Republic of Korea., Price S; Oxford University Hospitals NHS Foundation Trust, Oxford, OX3 7HE, UK., Schnur RE; GeneDx, Gaithersburg, MD 20877, USA., Douglas G; GeneDx, Gaithersburg, MD 20877, USA., Wentzensen IM; GeneDx, Gaithersburg, MD 20877, USA., Zweier C; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, 91054, Germany., Reis A; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, 91054, Germany., Bialer MG; Northwell Health, Division of Medical Genetics and Genomics, Great Neck, NY 11021, USA., Moore C; Northwell Health, Division of Medical Genetics and Genomics, Great Neck, NY 11021, USA., Koopmans M; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands., Brilstra EH; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands., Monroe GR; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands., van Gassen KLI; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands., van Binsbergen E; Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands., Newbury-Ecob R; University Hospitals Bristol, Department of Clinical Genetics, St Michael's Hospital, Bristol, BS2 8EG, UK., Bownass L; University Hospitals Bristol, Department of Clinical Genetics, St Michael's Hospital, Bristol, BS2 8EG, UK., Bader I; Department of Clinical Genetics, University Children's Hospital, Paracelsus Medical University, Salzburg, A-5020, Austria., Mayr JA; Department of Pediatrics, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, A-5020, Austria., Wortmann SB; Department of Pediatrics, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, A-5020, Austria.; Institute of Human Genetics, Technische Universität München, Munich, 81675, Germany.; Institute of Human Genetics, Helmholtz Zentrum München, Neuherberg, 85764, Germany., Jakielski KJ; Communication Sciences and Disorders, Augustana College, Rock Island, IL 61201, USA., Strand EA; Department of Neurology, Mayo Clinic, Rochester, MN 55905, USA., Kloth K; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany., Bierhals T; Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany., Roberts JD; National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA., Petrovich RM; National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA., Machida S; Waseda University, Tokyo, 169-8050, Japan., Kurumizaka H; Waseda University, Tokyo, 169-8050, Japan., Lelieveld S; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands., Pfundt R; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands., Jansen S; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands., Deriziotis P; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands., Faivre L; Equipe Génétique des Anomalies du Développement, Université de Bourgogne-Franche Comté, Dijon, 21070, France.; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon et Université de Bourgogne, Dijon, 21079, France., Thevenon J; Equipe Génétique des Anomalies du Développement, Université de Bourgogne-Franche Comté, Dijon, 21070, France.; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon et Université de Bourgogne, Dijon, 21079, France., Assoum M; Equipe Génétique des Anomalies du Développement, Université de Bourgogne-Franche Comté, Dijon, 21070, France.; Centre de Génétique et Centre de Référence Anomalies du Développement et Syndromes Malformatifs, FHU TRANSLAD, Hôpital d'Enfants, CHU Dijon et Université de Bourgogne, Dijon, 21079, France., Shriberg L; Waisman Center, Phonology Project, Madison, WI 53705-2280, USA., Kleefstra T; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands., Brunner HG; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands.; Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands., Wade PA; National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA., Fisher SE; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands. simon.fisher@mpi.nl.; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands. simon.fisher@mpi.nl., Campeau PM; CHU Sainte-Justine Research Center, Montreal, QC H3T 1C5, Canada. p.campeau@umontreal.ca.; Sainte-Justine Hospital, University of Montreal, Montreal, QC H3T 1C5, Canada. p.campeau@umontreal.ca. |
| Corporate Authors: | DDD study |
| Source: | Nature communications [Nat Commun] 2019 May 02; Vol. 10 (1), pp. 2079. Date of Electronic Publication: 2019 May 02. |
| Publication Type: | Published Erratum |
| Journal Info: | Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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