Referenced in: none

Automatically associated channels: Kir1.1 , Kir6.2

Title: Congenital hyperinsulinism due to a compound heterozygous ABCC8 mutation with spontaneous resolution at eight weeks.

Authors: Anitha Kumaran, Ritika R Kapoor, Sarah E Flanagan, Sian Ellard, Khalid Hussain

Journal, date & volume: Horm Res Paediatr, 2010 , 73, 287-92

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/20215776

Abstract