Referenced in: none

Automatically associated channels: Kir1.1 , Kir6.2

Title: The G53D mutation in Kir6.2 (KCNJ11) is associated with neonatal diabetes and motor dysfunction in adulthood that is improved with sulfonylurea therapy.

Authors: Joseph C Koster, Francesco Cadario, Cinzia Peruzzi, Carlo Colombo, Colin G Nichols, Fabrizio Barbetti

Journal, date & volume: J. Clin. Endocrinol. Metab., 2008 Mar , 93, 1054-61

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/18073297

Abstract