Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation. Issue 4 (27th March 2019)

Record Type:: Journal Article
Title:: Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation. Issue 4 (27th March 2019)
Main Title:: Complete clinical resolution of a Japanese family with renal pseudohypoaldosteronism type 1 due to a novel NR3C2 mutation
Authors:: Tanaka, Tatsuhiko
Oki, Eishin
Mori, Takayasu
Tsuruga, Kazushi
Sohara, Eisei
Uchida, Shinichi
Tanaka, Hiroshi
Abstract:
Is Part Of:: Nephrology. Volume 24:Issue 4(2019)
Journal:: Nephrology
Issue:: Volume 24:Issue 4(2019)
Issue Display:: Volume 24, Issue 4 (2019)
Year:: 2019
Volume:: 24
Issue:: 4
Issue Sort Value:: 2019-0024-0004-0000
Page Start:: 489
Page End:: 490
Publication Date:: 2019-03-27
Subjects:: Nephrology -- Periodicals
Kidneys -- Diseases -- Periodicals
Nephrologists -- Periodicals
616.61
616.61
Journal URLs:: http://onlinelibrary.wiley.com/ ↗
DOI:: 10.1111/nep.13391 ↗
Languages:: English
ISSNs:: 1320-5358
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 6075.684400
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store
Ingest File:: 9743.xml