Referenced in: none

Automatically associated channels: ClC4 , ClCK2

Title: Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafness.

Authors: Pierre Robitaille, Aicha Merouani, Ning He, York Pei

Journal, date & volume: Eur. J. Pediatr., 2011 Sep , 170, 1209-11

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/21479528

Abstract