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Correction: CDK13-related disorder: a deep characterization of speech and language abilities and addition of 33 novel cases.

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第一作者: Lottie D,Morison
第一单位: Speech and Language, Murdoch Children's Research Institute, Melbourne, VIC, Australia.
作者单位: Speech and Language, Murdoch Children's Research Institute, Melbourne, VIC, Australia. [1] Speech and Language, Murdoch Children's Research Institute, Melbourne, VIC, Australia.;School of Psychological Sciences, Monash University, Melbourne, VIC, Australia. [2] Génétique Clinique, Départment de Génétique Médicale, Maladies Rares et Médecine Personnalisée, CHU Montpellier, Montpellier University, Centre de Référence Anomalies du Développement SOOR, Montpellier, France. [3] Centre de Référence Anomalies du Développment et Syndromes Malformatifs, FHU TRANSLAD, CHU Dijon, Dijon, France.;Genetics of Developmental Disorders, INSERM - Bourgogne Franche-Comté Univeristy, Dijon, France. [4] Cancer Council Victoria, Melbourne, VIC, Australia. [5] Service de génétique médicale, CHU Nantes, 9 quai Moncousu, Nantes, France. [6] Unit of Medical Genetics, CHU La Réunion, Saint Pierre, France. [7] Lucile Packard Children's Hospital, Stanford Children's Health, Palo Alto, CA, USA. [8] Speech and Language, Murdoch Children's Research Institute, Melbourne, VIC, Australia.;Department of Paediatrics, The University of Melbourne, Melbourne, VIC, Australia.;The Royal Children's Hospital, Melbourne, VIC, Australia. [9] Speech and Language, Murdoch Children's Research Institute, Melbourne, VIC, Australia. angela.morgan@mcri.edu.au.;The Royal Children's Hospital, Melbourne, VIC, Australia. angela.morgan@mcri.edu.au.;Department of Audiology and Speech Pathology, The University of Melbourne, Melbourne, VIC, Australia. angela.morgan@mcri.edu.au. [10]
DOI 10.1038/s41431-023-01515-5
PMID 38066173
发布时间 2023-12-19
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European journal of human genetics : EJHG

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