Referenced in: none

Automatically associated channels: Kir1.1

Title: A novel mutation in KCNJ1 in a Bartter syndrome case diagnosed as pseudohypoaldosteronism.

Authors: Kandai Nozu, Xue Jun Fu, Hiroshi Kaito, Kyoko Kanda, Naoki Yokoyama, Rafal Przybyslaw Krol, Toshihiro Nakajima, Mizutaka Kajiyama, Kazumoto Iijima, Masafumi Matsuo

Journal, date & volume: Pediatr. Nephrol., 2007 Aug , 22, 1219-23

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/17401586

Abstract