Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.

Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
15 02 2019
Historique:
entrez: 17 2 2019
pubmed: 17 2 2019
medline: 17 2 2019
Statut: epublish

Résumé

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.

Identifiants

DOI: 10.1038/s41467-019-08800-2 PMID: 30770872 PMC: PMC6377600
pubmed: 30770872
doi: 10.1038/s41467-019-08800-2
pii: 10.1038/s41467-019-08800-2
pmc: PMC6377600
doi:

Types de publication

Journal Article Published Erratum

Langues

eng

Pagination

883

Subventions

Organisme : Medical Research Council
ID : MC_PC_16018
Pays : United Kingdom

Investigateurs

Jeremy F McRae (JF)
Stephen Clayton (S)
Tomas W Fitzgerald (TW)
Joanna Kaplanis (J)
Elena Prigmore (E)
Diana Rajan (D)
Alejandro Sifrim (A)
Stuart Aitken (S)
Nadia Akawi (N)
Mohsan Alvi (M)
Kirsty Ambridge (K)
Daniel M Barrett (DM)
Tanya Bayzetinova (T)
Philip Jones (P)
Wendy D Jones (WD)
Daniel King (D)
Netravathi Krishnappa (N)
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Tarjinder Singh (T)
Adrian R Tivey (AR)
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Uruj Anjum (U)
Hayley Archer (H)
Ruth Armstrong (R)
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Jonathan Berg (J)
Birgitta Bernhard (B)
A Paul Bevan (AP)
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John Burn (J)
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Commentaires et corrections

Type : ErratumFor

Auteurs

Lot Snijders Blok (LS)

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.
ORCID: 0000-0002-9825-3625

Justine Rousseau (J)

CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada.

Joanna Twist (J)

National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.

Sophie Ehresmann (S)

CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada.

Motoki Takaku (M)

National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.

Hanka Venselaar (H)

Centre for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.

Lance H Rodan (LH)

Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.

Catherine B Nowak (CB)

Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.

Jessica Douglas (J)

Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.

Kathryn J Swoboda (KJ)

Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.

Marcie A Steeves (MA)

Department of Medical Genetics, Massachusetts General Hospital, Boston, MA, 02114, USA.

Inderneel Sahai (I)

Department of Medical Genetics, Massachusetts General Hospital, Boston, MA, 02114, USA.

Connie T R M Stumpel (CTRM)

Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands.

Alexander P A Stegmann (APA)

Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands.

Patricia Wheeler (P)

Nemours Childrens Clinic, Orlando, FL, 32827, USA.

Marcia Willing (M)

Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, 63110, USA.

Elise Fiala (E)

Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, 63110, USA.

Aaina Kochhar (A)

Valley Children's Hospital, Madera, CA, 93636, USA.

William T 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.

Ana S A 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.
ORCID: 0000-0002-6353-6350

Ruky 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.

A Micheil 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.
ORCID: 0000-0001-9881-5467

P Y Billie 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.

Julia Rankin (J)

Department of Clinical Genetics, Royal Devon and Exeter NHS Foundation Trust (Heavitree), Exeter, EX2 5DW, UK.

Ilse J Anderson (IJ)

Division of Genetics, Department of Medicine, University of Tennessee Medical Center, Knoxville, TN, 37920, USA.

Steven A Skinner (SA)

Greenwood Genetic Center, Greenwood, SC, 29646, USA.

Raymond J Louie (RJ)

Greenwood Genetic Center, Greenwood, SC, 29646, USA.

Hannah E Warren (HE)

Greenwood Genetic Center, Greenwood, SC, 29646, USA.

Alexandra 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.

Boris 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.

Caroline 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.

Julien Buratti (J)

AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France.

Arnaud 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.

Diana 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.

Raymond Lewandowski (R)

Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA, 23298, USA.

Jennifer Propst (J)

Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA, 23298, USA.

Ton van Essen (T)

Clinical Genetics Department, University Medical Center Groningen, Groningen, 9700RB, The Netherlands.

Murim Choi (M)

Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea.

Sangmoon Lee (S)

Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea.

Jong H Chae (JH)

Department of Pediatrics, Seoul National University College of Medicine, Seoul National University Children's Hospital, Seoul, 08826, Republic of Korea.

Susan Price (S)

Oxford University Hospitals NHS Foundation Trust, Oxford, OX3 7HE, UK.

Rhonda E Schnur (RE)

GeneDx, Gaithersburg, MD, 20877, USA.

Ganka Douglas (G)

GeneDx, Gaithersburg, MD, 20877, USA.

Ingrid M Wentzensen (IM)

GeneDx, Gaithersburg, MD, 20877, USA.

Christiane Zweier (C)

Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, 91054, Germany.

André Reis (A)

Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, 91054, Germany.

Martin G Bialer (MG)

Northwell Health, Division of Medical Genetics and Genomics, Great Neck NY, 11021, USA.

Christine Moore (C)

Northwell Health, Division of Medical Genetics and Genomics, Great Neck NY, 11021, USA.

Marije Koopmans (M)

Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands.

Eva H Brilstra (EH)

Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands.

Glen R Monroe (GR)

Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands.

Koen L I van Gassen (KLI)

Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands.

Ellen van Binsbergen (E)

Department of Genetics, University Medical Center Utrecht, Utrecht University, Utrecht, 3508AB, The Netherlands.

Ruth Newbury-Ecob (R)

University Hospitals Bristol, Department of Clinical Genetics, St Michael's Hospital, Bristol, BS2 8EG, UK.

Lucy Bownass (L)

University Hospitals Bristol, Department of Clinical Genetics, St Michael's Hospital, Bristol, BS2 8EG, UK.

Ingrid Bader (I)

Department of Clinical Genetics, University Children's Hospital, Paracelsus Medical University, Salzburg, A-5020, Austria.

Johannes A Mayr (JA)

Department of Pediatrics, Salzburger Landeskliniken and Paracelsus Medical University, Salzburg, A-5020, Austria.

Saskia B 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.

Kathy J Jakielski (KJ)

Communication Sciences and Disorders, Augustana College, Rock Island, IL, 61201, USA.

Edythe A Strand (EA)

Department of Neurology, Mayo Clinic, Rochester, MN, 55905, USA.

Katja Kloth (K)

Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany.

Tatjana Bierhals (T)

Institute of Human Genetics, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany.

John D Roberts (JD)

National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.

Robert M Petrovich (RM)

National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.

Shinichi Machida (S)

Waseda University, Tokyo, 169-8050, Japan.

Hitoshi Kurumizaka (H)

Waseda University, Tokyo, 169-8050, Japan.
ORCID: 0000-0001-7412-3722

Stefan Lelieveld (S)

Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.

Rolph Pfundt (R)

Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.

Sandra 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.

Pelagia Deriziotis (P)

Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands.

Laurence 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.

Julien 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.

Mirna 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.

Lawrence Shriberg (L)

Waisman Center, Phonology Project, Madison, WI, 53705-2280, USA.

Tjitske 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.

Han G 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.

Paul A Wade (PA)

National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.
ORCID: 0000-0002-6042-357X

Simon E 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.
ORCID: 0000-0002-3132-1996

Philippe M 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.
ORCID: 0000-0001-9713-7107

Classifications MeSH