Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome.

Journal: American Journal of Human Genetics

Published: 2018-11-05

DOI: 10.1016/j.ajhg.2018.10.010

Affiliations: 16

Authors: 17

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Institutions FC
St. Louis Children's Hospital, United States of America (USA) 0.20
Edward Mallinckrodt Department of Pediatrics, WUSTL, United States of America (USA) 0.20
Department of Genome Sciences, UW, United States of America (USA) 0.15
Center for Human Nutrition, UT Southwestern Medical Center, United States of America (USA) 0.09
Division of Nutrition and Metabolic Diseases, UT Southwestern Medical Center, United States of America (USA) 0.06
Division of Medical Genetics and Metabolism, CHKD, United States of America (USA) 0.06
Department of Pediatrics, EVMS, United States of America (USA) 0.06
Department of Pediatrics, UT Southwestern Medical Center, United States of America (USA) 0.03
Genetic Health Queensland (GHQ), Australia 0.03
Royal Brisbane and Women's Hospital (RBWH), Australia 0.03
Department of Pediatrics, UW, United States of America (USA) 0.03
Eugene McDermott Center for Human Growth and Development, UT Southwestern Medical Center, United States of America (USA) 0.02
Lyda Hill Department of Bioinformatics, UT Southwestern Medical Center, United States of America (USA) 0.02
Department of Clinical Sciences, UT Southwestern Medical Center, United States of America (USA) 0.02
Department of Obstetrics and Gynecology (OB/GYN), WUSTL, United States of America (USA) 0.02

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