Nature Communications (Feb 2019)
Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
- Lot Snijders Blok,
- Justine Rousseau,
- Joanna Twist,
- Sophie Ehresmann,
- Motoki Takaku,
- Hanka Venselaar,
- Lance H. Rodan,
- Catherine B. Nowak,
- Jessica Douglas,
- Kathryn J. Swoboda,
- Marcie A. Steeves,
- Inderneel Sahai,
- Connie T. R. M. Stumpel,
- Alexander P. A. Stegmann,
- Patricia Wheeler,
- Marcia Willing,
- Elise Fiala,
- Aaina Kochhar,
- William T. Gibson,
- Ana S. A. Cohen,
- Ruky Agbahovbe,
- A. Micheil Innes,
- P. Y. Billie Au,
- Julia Rankin,
- Ilse J. Anderson,
- Steven A. Skinner,
- Raymond J. Louie,
- Hannah E. Warren,
- Alexandra Afenjar,
- Boris Keren,
- Caroline Nava,
- Julien Buratti,
- Arnaud Isapof,
- Diana Rodriguez,
- Raymond Lewandowski,
- Jennifer Propst,
- Ton van Essen,
- Murim Choi,
- Sangmoon Lee,
- Jong H. Chae,
- Susan Price,
- Rhonda E. Schnur,
- Ganka Douglas,
- Ingrid M. Wentzensen,
- Christiane Zweier,
- André Reis,
- Martin G. Bialer,
- Christine Moore,
- Marije Koopmans,
- Eva H. Brilstra,
- Glen R. Monroe,
- Koen L. I. van Gassen,
- Ellen van Binsbergen,
- Ruth Newbury-Ecob,
- Lucy Bownass,
- Ingrid Bader,
- Johannes A. Mayr,
- Saskia B. Wortmann,
- Kathy J. Jakielski,
- Edythe A. Strand,
- Katja Kloth,
- Tatjana Bierhals,
- The DDD study,
- John D. Roberts,
- Robert M. Petrovich,
- Shinichi Machida,
- Hitoshi Kurumizaka,
- Stefan Lelieveld,
- Rolph Pfundt,
- Sandra Jansen,
- Pelagia Deriziotis,
- Laurence Faivre,
- Julien Thevenon,
- Mirna Assoum,
- Lawrence Shriberg,
- Tjitske Kleefstra,
- Han G. Brunner,
- Paul A. Wade,
- Simon E. Fisher,
- Philippe M. Campeau
Affiliations
- Lot Snijders Blok
- Department of Human Genetics, Radboud University Medical Center
- Justine Rousseau
- CHU Sainte-Justine Research Center
- Joanna Twist
- National Institute of Environmental Health Sciences
- Sophie Ehresmann
- CHU Sainte-Justine Research Center
- Motoki Takaku
- National Institute of Environmental Health Sciences
- Hanka Venselaar
- Centre for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center
- Lance H. Rodan
- Division of Genetics and Genomics, Boston Children’s Hospital
- Catherine B. Nowak
- Division of Genetics and Genomics, Boston Children’s Hospital
- Jessica Douglas
- Division of Genetics and Genomics, Boston Children’s Hospital
- Kathryn J. Swoboda
- Department of Neurology, Massachusetts General Hospital and Harvard Medical School
- Marcie A. Steeves
- Department of Medical Genetics, Massachusetts General Hospital
- Inderneel Sahai
- Department of Medical Genetics, Massachusetts General Hospital
- Connie T. R. M. Stumpel
- Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center
- Alexander P. A. Stegmann
- Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center
- Patricia Wheeler
- Nemours Childrens Clinic
- Marcia Willing
- Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine
- Elise Fiala
- Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine
- Aaina Kochhar
- Valley Children’s Hospital
- William T. Gibson
- British Columbia Children’s Hospital Research Institute
- Ana S. A. Cohen
- British Columbia Children’s Hospital Research Institute
- Ruky Agbahovbe
- British Columbia Children’s Hospital Research Institute
- A. Micheil Innes
- Department of Medical Genetics and Alberta Children’s Hospital Research Institute, Cumming School of Medicine, University of Calgary
- P. Y. Billie Au
- Department of Medical Genetics and Alberta Children’s Hospital Research Institute, Cumming School of Medicine, University of Calgary
- Julia Rankin
- Department of Clinical Genetics, Royal Devon and Exeter NHS Foundation Trust (Heavitree)
- Ilse J. Anderson
- Division of Genetics, Department of Medicine, University of Tennessee Medical Center
- Steven A. Skinner
- Greenwood Genetic Center
- Raymond J. Louie
- Greenwood Genetic Center
- Hannah E. Warren
- Greenwood Genetic Center
- Alexandra Afenjar
- 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
- Boris Keren
- AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique
- Caroline Nava
- AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique
- Julien Buratti
- AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique
- Arnaud Isapof
- 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
- Diana Rodriguez
- GRC ConCer-LD, Sorbonne Universités, UPMC Univ Paris 06; Department of Child Neurology and National Reference Center for Neurogenetic Disorders, Armand Trousseau Hospital, GHUEP
- Raymond Lewandowski
- Clinical Genetics Division, Virginia Commonwealth University Health System
- Jennifer Propst
- Clinical Genetics Division, Virginia Commonwealth University Health System
- Ton van Essen
- Clinical Genetics Department, University Medical Center Groningen
- Murim Choi
- Department of Biomedical Sciences, Seoul National University College of Medicine
- Sangmoon Lee
- Department of Biomedical Sciences, Seoul National University College of Medicine
- Jong H. Chae
- Department of Pediatrics, Seoul National University College of Medicine, Seoul National University Children’s Hospital
- Susan Price
- Oxford University Hospitals NHS Foundation Trust
- Rhonda E. Schnur
- GeneDx
- Ganka Douglas
- GeneDx
- Ingrid M. Wentzensen
- GeneDx
- Christiane Zweier
- Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg
- André Reis
- Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg
- Martin G. Bialer
- Northwell Health, Division of Medical Genetics and Genomics
- Christine Moore
- Northwell Health, Division of Medical Genetics and Genomics
- Marije Koopmans
- Department of Genetics, University Medical Center Utrecht, Utrecht University
- Eva H. Brilstra
- Department of Genetics, University Medical Center Utrecht, Utrecht University
- Glen R. Monroe
- Department of Genetics, University Medical Center Utrecht, Utrecht University
- Koen L. I. van Gassen
- Department of Genetics, University Medical Center Utrecht, Utrecht University
- Ellen van Binsbergen
- Department of Genetics, University Medical Center Utrecht, Utrecht University
- Ruth Newbury-Ecob
- University Hospitals Bristol, Department of Clinical Genetics, St Michael’s Hospital
- Lucy Bownass
- University Hospitals Bristol, Department of Clinical Genetics, St Michael’s Hospital
- Ingrid Bader
- Department of Clinical Genetics, University Children’s Hospital, Paracelsus Medical University
- Johannes A. Mayr
- Department of Pediatrics, Salzburger Landeskliniken and Paracelsus Medical University
- Saskia B. Wortmann
- Department of Pediatrics, Salzburger Landeskliniken and Paracelsus Medical University
- Kathy J. Jakielski
- Communication Sciences and Disorders, Augustana College
- Edythe A. Strand
- Department of Neurology, Mayo Clinic
- Katja Kloth
- Institute of Human Genetics, University Medical Center Hamburg-Eppendorf
- Tatjana Bierhals
- Institute of Human Genetics, University Medical Center Hamburg-Eppendorf
- The DDD study
- John D. Roberts
- National Institute of Environmental Health Sciences
- Robert M. Petrovich
- National Institute of Environmental Health Sciences
- Shinichi Machida
- Waseda University
- Hitoshi Kurumizaka
- Waseda University
- Stefan Lelieveld
- Department of Human Genetics, Radboud University Medical Center
- Rolph Pfundt
- Department of Human Genetics, Radboud University Medical Center
- Sandra Jansen
- Department of Human Genetics, Radboud University Medical Center
- Pelagia Deriziotis
- Language and Genetics Department, Max Planck Institute for Psycholinguistics
- Laurence Faivre
- Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté
- Julien Thevenon
- Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté
- Mirna Assoum
- Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté
- Lawrence Shriberg
- Waisman Center, Phonology Project
- Tjitske Kleefstra
- Department of Human Genetics, Radboud University Medical Center
- Han G. Brunner
- Department of Human Genetics, Radboud University Medical Center
- Paul A. Wade
- National Institute of Environmental Health Sciences
- Simon E. Fisher
- Language and Genetics Department, Max Planck Institute for Psycholinguistics
- Philippe M. Campeau
- CHU Sainte-Justine Research Center
- DOI
- https://doi.org/10.1038/s41467-019-08800-2
- Journal volume & issue
-
Vol. 10,
no. 1
pp. 1 – 4
Abstract
The original version of this Article contained an error in the spelling of the author Laurence Faivre, which was incorrectly given as Laurence Faive. This has now been corrected in both the PDF and HTML versions of the Article.
