Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy

Journal: Nature Genetics

Published: 2018-02-26

DOI: 10.1038/s41588-018-0063-6

Affiliations: 19

Authors: 24

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Institutions FC
Department of Pediatrics, LMU, Germany 0.42
Oslo University Hospital (OUS), Norway 0.15
Division of Gastroenterology, Hepatology and Nutrition, BCH, United States of America (USA) 0.07
UiO Faculty of Medicine, Norway 0.06
Translational Gastroenterology Unit (TGU), United Kingdom (UK) 0.04
Institute of Pathology, LMU, Germany 0.04
University of Malaya Medical Centre (UMMC), Malaysia 0.04
UiO Department of Medical Genetics (DMG), Norway 0.04
Harvard Medical School (HMS), United States of America (USA) 0.03
Gene Center Munich, LMU, Germany 0.02
Department of Biochemistry (BC), LMU, Germany 0.02
Department of Pediatric Newborn Medicine, BWH, United States of America (USA) 0.01
Division of Gastroenterology, Hepatology and Endoscopy, BWH, United States of America (USA) 0.01
Inflammatory Bowel Disease Center (IBD), SickKids U of T, Canada 0.01
SickKids Research Institute, SickKids U of T, Canada 0.01
Division of Gastroenterology, Hepatology, and Nutrition, SickKids U of T, Canada 0.01
Department of Biochemistry, U of T, Canada 0.01

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