Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

Journal: American Journal of Human Genetics

Published: 2021-02-04

DOI: 10.1016/j.ajhg.2021.01.007

Affiliations: 31

Authors: 20

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Institutions Share
University of Lausanne (UNIL), Switzerland 0.15
Radboud University Medical Centre (Radboudumc), RU, Netherlands 0.10
Donders Institute for Brain, Cognition and Behaviour, Netherlands 0.07
The University of Utah (Utah), United States of America (USA) 0.05
Vilnius University (VU), Lithuania 0.05
Manchester Centre for Genomic Medicine (MCGM), United Kingdom (UK) 0.05
Geneva University Hospitals (HUG), Switzerland 0.05
Hospital Kuala Lumpur (HKL), Malaysia 0.05
Technical University of Munich (TUM), Germany 0.05
University of Oxford, United Kingdom (UK) 0.04
Max Planck Institute for Psycholinguistics, Netherlands 0.03
Donald and Barbara Zucker School of Medicine at Hofstra/Northwell, United States of America (USA) 0.03
The George Washington University (GW), United States of America (USA) 0.03
Children's National Health System, United States of America (USA) 0.03
Tel Aviv University (TAU), Israel 0.03
Feinstein Institutes for Medical Research, Northwell Health, United States of America (USA) 0.03
International Max Planck Research School for Language Sciences (IMPRS for Language Sciences), Netherlands 0.03
Edmond and Lily Safra Children's Hospital, Chaim Sheba Medical Center, Israel 0.03
Children’s Mercy Kansas City, United States of America (USA) 0.03
University of Missouri-Kansas City (UMKC), United States of America (USA) 0.03
Lipids, Nutrition, Cancer (LNC), France 0.02
Genetics of Development Disorders Team (GAD), France 0.02
Dijon University Hospital, France 0.02
Radboud Institute for Molecular Life Sciences (RIMLS), RU, Netherlands 0.02
Maastricht University Medical Center+ (Maastricht UMC+), Netherlands 0.02
John Radcliffe Hospital, United Kingdom (UK) 0.01

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