Referenced in: none

Automatically associated channels: Kir1.1 , Kir6.2

Title: Heterozygous mutations of the gene for Kir 1.1 (ROMK) in antenatal Bartter syndrome presenting with transient hyperkalemia, evolving to a benign course.

Authors: Jong Tae Cho, Lisa Marie Guay-Woodford

Journal, date & volume: J. Korean Med. Sci., 2003 Feb , 18, 65-8

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/12589089

Abstract