Referenced in: none

Automatically associated channels: ClC4 , ClCK2

Title: A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain.

Authors: Juan Rodríguez-Soriano, Alfredo Vallo, Gustavo Pérez de Nanclares, José Ramón Bilbao, Luis Castano

Journal, date & volume: Pediatr. Nephrol., 2005 Jul , 20, 891-6

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/15875219

Abstract