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Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language.
Blok, Lot Snijders; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H; Nowak, Catherine B; Douglas, Jessica; Swoboda, Kathryn J; Steeves, Marcie A; Sahai, Inderneel; Stumpel, Connie T R M; Stegmann, Alexander P A; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T; Cohen, Ana S A; Agbahovbe, Ruky; Innes, A Micheil; Au, P Y Billie; Rankin, Julia; Anderson, Ilse J; Skinner, Steven A; Louie, Raymond J; Warren, Hannah E; Afenjar, Alexandra; Keren, Boris; Nava, Caroline; Buratti, Julien; Isapof, Arnaud; Rodriguez, Diana; Lewandowski, Raymond; Propst, Jennifer; van Essen, Ton; Choi, Murim; Lee, Sangmoon; Chae, Jong H; Price, Susan; Schnur, Rhonda E; Douglas, Ganka; Wentzensen, Ingrid M; Zweier, Christiane; Reis, André; Bialer, Martin G; Moore, Christine; Koopmans, Marije; Brilstra, Eva H.
Afiliación
  • Blok LS; Department of Human Genetics, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.
  • Rousseau J; Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, 6500AH, The Netherlands.
  • Twist J; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, 6500HE, The Netherlands.
  • 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; CHU Sainte-Justine Research Center, Montreal, QC, H3T 1C5, Canada.
  • Rodan LH; National Institute of Environmental Health Sciences, Research Triangle Park, NC, 27709, USA.
  • Nowak CB; Centre for Molecular and Biomolecular Informatics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, 6500HB, The Netherlands.
  • Douglas J; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.
  • Swoboda KJ; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.
  • Steeves MA; Division of Genetics and Genomics, Boston Children's Hospital, Boston, MA, 02115, USA.
  • Sahai I; Department of Neurology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, 02114, USA.
  • Stumpel CTRM; Department of Medical Genetics, Massachusetts General Hospital, Boston, MA, 02114, USA.
  • Stegmann APA; Department of Medical Genetics, Massachusetts General Hospital, Boston, MA, 02114, USA.
  • Wheeler P; Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands.
  • Willing M; Department of Clinical Genetics and GROW-School for Oncology and Developmental Biology, Maastricht University Medical Center, Maastricht, 6202AZ, The Netherlands.
  • Fiala E; Nemours Childrens Clinic, Orlando, FL, 32827, USA.
  • Kochhar A; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, 63110, USA.
  • Gibson WT; Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine, St. Louis, MO, 63110, USA.
  • Cohen ASA; Valley Children's Hospital, Madera, CA, 93636, USA.
  • Agbahovbe R; British Columbia Children's Hospital Research Institute, Vancouver, BC, V5Z 4H4, Canada.
  • Innes AM; Department of Medical Genetics, University of British Columbia, Vancouver, BC, V6H 3N1, Canada.
  • Au PYB; British Columbia Children's Hospital Research Institute, Vancouver, BC, V5Z 4H4, Canada.
  • Rankin J; Department of Medical Genetics, University of British Columbia, Vancouver, BC, V6H 3N1, Canada.
  • Anderson IJ; British Columbia Children's Hospital Research Institute, Vancouver, BC, V5Z 4H4, Canada.
  • Skinner SA; Department of Medical Genetics, University of British Columbia, Vancouver, BC, V6H 3N1, Canada.
  • Louie RJ; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, T2N 4N1, Canada.
  • Warren HE; Department of Medical Genetics and Alberta Children's Hospital Research Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, T2N 4N1, Canada.
  • Afenjar A; Department of Clinical Genetics, Royal Devon and Exeter NHS Foundation Trust (Heavitree), Exeter, EX2 5DW, UK.
  • Keren B; Division of Genetics, Department of Medicine, University of Tennessee Medical Center, Knoxville, TN, 37920, USA.
  • Nava C; Greenwood Genetic Center, Greenwood, SC, 29646, USA.
  • Buratti J; Greenwood Genetic Center, Greenwood, SC, 29646, USA.
  • Isapof A; Greenwood Genetic Center, Greenwood, SC, 29646, USA.
  • Rodriguez D; 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.
  • Lewandowski R; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France.
  • Propst J; Groupe de Recherche Clinique (GRC) 'déficience intellectuelle et autisme' UPMC, Paris, 75005, France.
  • van Essen T; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France.
  • Choi M; Groupe de Recherche Clinique (GRC) 'déficience intellectuelle et autisme' UPMC, Paris, 75005, France.
  • Lee S; 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.
  • Chae JH; AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique, Paris, 75013, France.
  • Price S; 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.
  • Schnur RE; 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.
  • Douglas G; Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA, 23298, USA.
  • Wentzensen IM; Clinical Genetics Division, Virginia Commonwealth University Health System, Richmond, VA, 23298, USA.
  • Zweier C; Clinical Genetics Department, University Medical Center Groningen, Groningen, 9700RB, The Netherlands.
  • Reis A; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea.
  • Bialer MG; Department of Biomedical Sciences, Seoul National University College of Medicine, Seoul, 08826, Republic of Korea.
  • Moore C; Department of Pediatrics, Seoul National University College of Medicine, Seoul National University Children's Hospital, Seoul, 08826, Republic of Korea.
  • Koopmans M; Oxford University Hospitals NHS Foundation Trust, Oxford, OX3 7HE, UK.
  • Brilstra EH; GeneDx, Gaithersburg, MD, 20877, USA.
Nat Commun ; 10(1): 883, 2019 02 15.
Article en En | MEDLINE | ID: mdl-30770872
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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2019 Tipo del documento: Article País de afiliación: Países Bajos
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2019 Tipo del documento: Article País de afiliación: Países Bajos