Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in <it>MR </it>gene

Autosomal dominant pseudohypoaldosteronism type 1 with a novel splice site mutation in <it>MR </it>gene

<p>Abstract</p> <p>Background</p> <p>Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) is a rare inherited condition that is characterized by renal resistance to aldosterone as well as salt wasting, hyperkalemia, and metabolic acidosis. Renal PHA1 is caused by mu...

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Bibliographic Details
Main Authors:	Kaito Hiroshi, Hashimura Yuya, Miwa Akihiro, Morioka Ichiro, Yokoyama Naoki, Nozu Kandai, Kanda Kyoko, Iijima Kazumoto, Matsuo Masafumi
Format:	Article
Language:	English
Published:	BMC 2009-11-01
Series:	BMC Nephrology
Online Access:	http://www.biomedcentral.com/1471-2369/10/37

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