Referenced in: none

Automatically associated channels: Kir1.1 , Kir6.2

Title: Kir6.2 mutations are a common cause of permanent neonatal diabetes in a large cohort of French patients.

Authors: Martine Vaxillaire, Céline Populaire, Kanetee Busiah, Hélène Cavé, Anna L Gloyn, Andrew T Hattersley, Paul Czernichow, Philippe Froguel, Michel Polak

Journal, date & volume: Diabetes, 2004 Oct , 53, 2719-22

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/15448107

Abstract