Referenced in: none

Automatically associated channels: Kir1.1 , Kir2.3 , Kir6.2

Title: A syndrome of congenital hyperinsulinism and rhabdomyolysis is caused by KCNJ11 mutation.

Authors: Mamdouh Albaqumi, Fatimah A Alhabib, Hanan E Shamseldin, Firdous Mohammed, Fowzan S Alkuraya

Journal, date & volume: J. Med. Genet., 2014 Apr , 51, 271-4

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/24421282

Abstract