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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
    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 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

    (University of Calgary)

  • P. Y. Billie Au

    (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
    UPMC Univ Paris 06 UMR S 1127)

  • Julien Buratti

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

  • Arnaud Isapof

    (Armand Trousseau Hospital, GHUEP, AP-HP)

  • Diana Rodriguez

    (Armand Trousseau Hospital, GHUEP, AP-HP, INSERM U1141)

  • 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

    (Division of Medical Genetics and Genomics)

  • Christine Moore

    (Division of Medical Genetics and Genomics)

  • Marije Koopmans

    (Utrecht University)

  • Eva H. Brilstra

    (Utrecht University)

  • Glen R. Monroe

    (Utrecht University)

  • Koen L. I. Gassen

    (Utrecht University)

  • Ellen Binsbergen

    (Utrecht University)

  • Ruth Newbury-Ecob

    (St Michael’s Hospital)

  • Lucy Bownass

    (St Michael’s Hospital)

  • Ingrid Bader

    (Paracelsus Medical University)

  • Johannes A. Mayr

    (Salzburger Landeskliniken and Paracelsus Medical University)

  • Saskia B. Wortmann

    (Salzburger Landeskliniken and Paracelsus Medical University
    Technische Universität München
    Helmholtz Zentrum München)

  • Kathy J. Jakielski

    (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
    Radboud University)

  • Pelagia Deriziotis

    (Max Planck Institute for Psycholinguistics)

  • Laurence Faivre

    (Université de Bourgogne-Franche Comté
    CHU Dijon et Université de Bourgogne)

  • Julien Thevenon

    (Université de Bourgogne-Franche Comté
    CHU Dijon et Université de Bourgogne)

  • Mirna Assoum

    (Université de Bourgogne-Franche Comté
    CHU Dijon et Université de Bourgogne)

  • Lawrence Shriberg

    (Phonology Project)

  • Tjitske Kleefstra

    (Radboud University Medical Center
    Radboud University)

  • Han G. Brunner

    (Radboud University Medical Center
    Radboud University
    Maastricht University Medical Center)

  • Paul A. Wade

    (National Institute of Environmental Health Sciences)

  • Simon E. Fisher

    (Max Planck Institute for Psycholinguistics
    Radboud University)

  • Philippe M. Campeau

    (CHU Sainte-Justine Research Center
    University of Montreal)

Abstract

The HTML and PDF versions of this Article were updated after publication to remove images of one individual from Figure 1.

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_s41467-019-10161-9
    DOI: 10.1038/s41467-019-10161-9
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