Referenced in: none

Automatically associated channels: ClC4 , ClC5 , Kir1.1

Title: A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency.

Authors: Radovan Bogdanović, Markus Draaken, Alma Toromanović, Maja Dordević, Natasa Stajić, Michael Ludwig

Journal, date & volume: Pediatr. Nephrol., 2010 Nov , 25, 2363-8

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/20680351

Abstract