학술논문
CLCN2 chloride channel mutations in familial hyperaldosteronism type II
Document Type
Article
Author
Scholl, U.I.; Schewe, J.; Thiel, A.; Rump, L.C.; Stölting, G.; Tan, H.; Untiet, V.; Fahlke, C.; Nelson-Williams, C.; Vichot, A.A.; Jin, S.C.; Loring, E.; Choi, J.; Lifton, R.P.; Yoo, T.; Choi, M.; Xu, S.; Wu, A.; Gordon, R.; Stowasser, M.; Kirchner, M.; Mertins, P.; Onder, A.M.; Gamble, C.; McKenney, D.; Lash, R.W.; Jones, D.P.; Chune, G.; Gagliardi, P.
Source
In: Nature Genetics . (Nature Genetics, 1 March 2018, 50(3):349-354)
Subject
Language
English
ISSN
15461718
10614036
10614036