Referenced in: none

Automatically associated channels: Kir1.1

Title: Mutations in the gene encoding the inwardly-rectifying renal potassium channel, ROMK, cause the antenatal variant of Bartter syndrome: evidence for genetic heterogeneity. International Collaborative Study Group for Bartter-like Syndromes.

Authors:

Journal, date & volume: Hum. Mol. Genet., 1997 Jan , 6, 17-26

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/9002665

Abstract