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Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation
Author(s) -
Tanaka Tatsuhiko,
Oki Eishin,
Mori Takayasu,
Tsuruga Kazushi,
Sohara Eisei,
Uchida Shinichi,
Tanaka Hiroshi
Publication year - 2019
Publication title -
nephrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.752
H-Index - 61
eISSN - 1440-1797
pISSN - 1320-5358
DOI - 10.1111/nep.13391
Subject(s) - pseudohypoaldosteronism , medicine , mutation , resolution (logic) , genetics , hyperkalemia , gene , artificial intelligence , biology , computer science
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