Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity

Journal: Nature Communications

Published: 2020-05-15

DOI: 10.1038/s41467-020-16294-6

Affiliations: 20

Authors: 28

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Institutions Share
Institute of Genetics and Molecular and Cellular Biology (IGBMC), France 0.27
Texas Children's Hospital, BCM, United States of America (USA) 0.07
Amsterdam UMC, Netherlands 0.07
Neurology and Neurogenetics Clinic, Kennedy Krieger Institute, United States of America (USA) 0.07
GeneDx Inc., United States of America (USA) 0.07
Department of Molecular and Human Genetics, BCM, United States of America (USA) 0.07
Grenoble Institute of Neuroscience (GIN), France 0.07
Research Center of the Brain and Spinal Cord Institute (CRISM), ICM, France 0.07
Département de Génétique, AP-HP Hôpitaux Universitaires La Pitié-Salpêtrière - Charles-Foix, France 0.05
Department of Neurology, BCH, United States of America (USA) 0.04
Centre Déficiences Intellectuelles de Causes Rares (CRDI-Paris), Service de Génétique Médicale, Hôpital Necker-Enfants Malades, France 0.03
GRC Déficience Intellectuelle et Autisme, Sorbonne Université, France 0.03
Fédération Hospitalo-Universitaire Médecine TRANSLationnelle et Anomalies du Développement (FHU-TRANSLAD), France 0.02
Reference Centre for Developmental Anomalies and Malformation Syndromes - Coordinator Site Bourgogne -1, Dijon University Hospital, France 0.02
Lipids, Nutrition, Cancer (LNC), France 0.01
Centre de Génétique - Centre de Référence des Maladies Rares, Anomalies du Développement et Syndromes Malformatifs et Déficiences Intellectuelles de Causes Rares, Dijon University Hospital, France 0.01
Institute of Human Genetics, UDE, Germany 0.01

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