Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities.

Journal: American Journal of Human Genetics

Published: 2020-01-25

DOI: 10.1016/j.ajhg.2020.01.002

Affiliations: 18

Authors: 25

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Institutions Share
TUM-HMGU Institute of Human Genetics (IHG), Germany 0.19
Department of General Paediatrics, HHU, Germany 0.16
Department of Medicine, UC San Diego, United States of America (USA) 0.08
UNC Department of Pediatrics, United States of America (USA) 0.08
Department of Genetics, KFSH&RC, Saudi Arabia 0.08
Sackler Faculty of Medicine, TAU, Israel 0.08
Edmond and Lily Safra Children's Hospital, Chaim Sheba Medical Center, Israel 0.06
The Sheba Cancer Research Center (SCRC), Chaim Sheba Medical Center, Israel 0.04
Levine Children's Hospital, Atrium Health, United States of America (USA) 0.04
Department of Paediatric Oncology, Haematology and Immunology, HHU, Germany 0.04
Institute of Human Genetics, HHU, Germany 0.04
Faculty of Medicine, HHU, Germany 0.04
Chaim Sheba Medical Center at Tel HaShomer, Israel 0.02
College of Medicine, KSAU-HS, Saudi Arabia 0.02
King Saud bin Abdulaziz University for Health Sciences (KSAU-HS), Saudi Arabia 0.02
Institute of Neurogenomics (ING), HMGU, Germany 0.01

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