CLCN2 chloride channel mutations in familial hyperaldosteronism type II

Journal: Nature Genetics

Published: 2018-02-05

DOI: 10.1038/s41588-018-0048-5

Affiliations: 17

Authors: 29

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Institutions FC
Institutsbereich Zelluläre Biophysik (ICS-4), FZJ, Germany 0.14
The University of Queensland Diamantina Institute (UQDI), UQ, Australia 0.14
Department of Nephrology, HHU, Germany 0.12
Yale Department of Genetics, United States of America (USA) 0.11
Berlin Institute of Health (BIH), Germany 0.09
Yale School of Medicine (YSM), United States of America (USA) 0.07
Department of Biomedical Sciences (BMS), SNU, South Korea 0.07
Le Bonheur Children's Hospital, UTHSC, United States of America (USA) 0.03
Cooper Clinic PA, United States of America (USA) 0.03
Peyton Manning Children's Hospital at St.Vincent, United States of America (USA) 0.03
Division of Metabolism, Endocrinology and Diabetes (MEND), U-M, United States of America (USA) 0.03
School of Medicine, VU, United States of America (USA) 0.03
Central Texas Veterans Health Care System (CTVHCS), United States of America (USA) 0.03
Nemours Children's Specialty Care, Jacksonville, United States of America (USA) 0.03
Yale Center for Mendelian Genomics (CMG), United States of America (USA) 0.02
Laboratory of Human Genetics and Genomics, The Rockefeller University, United States of America (USA) 0.01

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