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

Author

Listed:
  • Lot Snijders Blok

    (Radboud University Medical Center
    Max Planck Institute for Psycholinguistics
    Cognition and Behaviour, Radboud University)

  • 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

    (Radboud Institute for Molecular Life Sciences, Radboud University Medical Center)

  • Lance H. Rodan

    (Boston Children’s Hospital)

  • Catherine B. Nowak

    (Boston Children’s Hospital)

  • Jessica Douglas

    (Boston Children’s Hospital)

  • Kathryn J. Swoboda

    (Massachusetts General Hospital and Harvard Medical School)

  • Marcie A. Steeves

    (Massachusetts General Hospital)

  • Inderneel Sahai

    (Massachusetts General Hospital)

  • Connie T. R. M. Stumpel

    (Maastricht University Medical Center)

  • Alexander P. A. Stegmann

    (Maastricht University Medical Center)

  • Patricia Wheeler

    (Nemours Childrens Clinic)

  • Marcia Willing

    (Washington University School of Medicine)

  • Elise Fiala

    (Washington University School of Medicine)

  • Aaina Kochhar

    (Valley Children’s Hospital)

  • William T. Gibson

    (British Columbia Children’s Hospital Research Institute
    University of British Columbia)

  • Ana S. A. Cohen

    (British Columbia Children’s Hospital Research Institute
    University of British Columbia)

  • Ruky Agbahovbe

    (British Columbia Children’s Hospital Research Institute
    University of British Columbia)

  • A. Micheil Innes

    (Cumming School of Medicine, University of Calgary)

  • P. Y. Billie Au

    (Cumming School of Medicine, University of Calgary)

  • Julia Rankin

    (Royal Devon and Exeter NHS Foundation Trust (Heavitree))

  • Ilse J. Anderson

    (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

    (Armand Trousseau Hospital, GHUEP, AP-HP)

  • Boris Keren

    (AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique
    Groupe de Recherche Clinique (GRC) ‘déficience intellectuelle et autisme’ UPMC)

  • Caroline Nava

    (AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique
    Groupe de Recherche Clinique (GRC) ‘déficience intellectuelle et autisme’ UPMC
    INSERM, U 1127, CNRS UMR 7225, Institut du Cerveau et de la Moelle épinière, ICM, Sorbonne Universités)

  • Julien Buratti

    (AP-HP, Hôpital de la Pitié-Salpêtrière, Département de Génétique)

  • Arnaud Isapof

    (FILNEMUS, Armand Trousseau Hospital, GHUEP, AP-HP)

  • Diana Rodriguez

    (Armand Trousseau Hospital, GHUEP)

  • Raymond Lewandowski

    (Virginia Commonwealth University Health System)

  • Jennifer Propst

    (Virginia Commonwealth University Health System)

  • Ton Essen

    (University Medical Center Groningen)

  • Murim Choi

    (Seoul National University College of Medicine)

  • Sangmoon Lee

    (Seoul National University College of Medicine)

  • Jong H. Chae

    (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

    (Friedrich-Alexander-Universität Erlangen-Nürnberg)

  • André Reis

    (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

    (University Medical Center Utrecht, Utrecht University)

  • Eva H. Brilstra

    (University Medical Center Utrecht, Utrecht University)

  • Glen R. Monroe

    (University Medical Center Utrecht, Utrecht University)

  • Koen L. I. Gassen

    (University Medical Center Utrecht, Utrecht University)

  • Ellen Binsbergen

    (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

    (University Children’s Hospital, Paracelsus Medical University)

  • Johannes A. Mayr

    (Salzburger Landeskliniken and Paracelsus Medical University)

  • Saskia B. Wortmann

    (Salzburger Landeskliniken and Paracelsus Medical University
    Institute of Human Genetics, Technische Universität München
    Institute of Human Genetics, Helmholtz Zentrum München)

  • Kathy J. Jakielski

    (Communication Sciences and Disorders, Augustana College)

  • Edythe A. Strand

    (Mayo Clinic)

  • Katja Kloth

    (University Medical Center Hamburg-Eppendorf)

  • Tatjana Bierhals

    (University Medical Center Hamburg-Eppendorf)

  • 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

    (Radboud University Medical Center)

  • Rolph Pfundt

    (Radboud University Medical Center)

  • Sandra Jansen

    (Radboud University Medical Center
    Cognition and Behaviour, Radboud University)

  • Pelagia Deriziotis

    (Max Planck Institute for Psycholinguistics)

  • Laurence Faivre

    (Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté
    FHU TRANSLAD, Hôpital d’Enfants, CHU Dijon et Université de Bourgogne)

  • Julien Thevenon

    (Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté
    FHU TRANSLAD, Hôpital d’Enfants, CHU Dijon et Université de Bourgogne)

  • Mirna Assoum

    (Equipe Génétique des Anomalies du Développement, Université de Bourgogne- Franche Comté
    FHU TRANSLAD, Hôpital d’Enfants, CHU Dijon et Université de Bourgogne)

  • Lawrence Shriberg

    (Waisman Center, Phonology Project)

  • Tjitske Kleefstra

    (Radboud University Medical Center
    Cognition and Behaviour, Radboud University)

  • Han G. Brunner

    (Radboud University Medical Center
    Cognition and Behaviour, Radboud University
    Maastricht University Medical Center)

  • Paul A. Wade

    (National Institute of Environmental Health Sciences)

  • Simon E. Fisher

    (Max Planck Institute for Psycholinguistics
    Cognition and Behaviour, Radboud University)

  • Philippe M. Campeau

    (CHU Sainte-Justine Research Center
    Sainte-Justine Hospital, University of Montreal)

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.

Suggested Citation

  • 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. Steeve, 2019. "Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language," Nature Communications, Nature, vol. 10(1), pages 1-4, December.
    • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-08800-2
    DOI: 10.1038/s41467-019-08800-2
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