Referenced in: none

Automatically associated channels: ClC4 , ClC5 , Kir1.1

Title: A patient with Dent disease and features of Bartter syndrome caused by a novel mutation of CLCN5.

Authors: Takayuki Okamoto, Toshihiro Tajima, Tomoya Hirayama, Satoshi Sasaki

Journal, date & volume: Eur. J. Pediatr., 2012 Feb , 171, 401-4

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/21932010

Abstract