Referenced in: none

Automatically associated channels: ClC4 , ClCK2

Title: Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndrome.

Authors: Y Yu, C Xu, X Pan, H Ren, W Wang, X Meng, F Huang, N Chen

Journal, date & volume: Clin. Genet., 2010 Feb , 77, 155-62

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/19807735

Abstract