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Rare De Novo Missense Variants in RNA Helicase DDX6 Cause Intellectual Disability and Dysmorphic Features and Lead to P-Body Defects and RNA Dysregulation.

Journal: American Journal of Human Genetics

Published: 2019-08-05

DOI: 10.1016/j.ajhg.2019.07.010

Affiliations: 23

Authors: 38

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Institutions Share
Neurogenomics Division, TGen, United States of America (USA) 0.17
Center for Rare Childhood Disorders, TGen, United States of America (USA) 0.17
Developmental Biology Laboratory (LBD), IBPS, France 0.11
Institute of Genetics and Molecular and Cellular Biology (IGBMC), France 0.09
GeneDx Inc., United States of America (USA) 0.08
University Hospitals of Strasbourg (HUS), France 0.07
Laboratoire de Génétique Médicale (LGM), France 0.07
Department of Genetics, RUG, Netherlands 0.05
CEA National Center of Human Genomics Research (CNRGH), France 0.05
Analytic and Translational Genetics Unit (ATGU), MGH, United States of America (USA) 0.03
Stanley Center for Psychiatric Research, Broad Institute, United States of America (USA) 0.03
Department of Human Genetics, RU, Netherlands 0.03
Geisinger Medical Center, United States of America (USA) 0.03
Epilepsy Center, Cleveland Clinic, United States of America (USA) 0.01
University of Strasbourg Institute for Advanced Study (USIAS), France 0.01
Genomic Medicine Institute (GMI), Cleveland Clinic, United States of America (USA) 0
Lerner Research Institute, Cleveland Clinic, United States of America (USA) 0
Cologne Center for Genomics (CCG), UoC, Germany 0

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