Referenced in: none

Automatically associated channels: Kir1.1 , Kir6.2

Title: Characterization of the ABCC8 gene mutation and phenotype in patients with congenital hyperinsulinism in western Saudi Arabia.

Authors: Abdulmoein E Al-Agha, Ihab A Ahmad

Journal, date & volume: Saudi Med J, 2013 Oct , 34, 1002-6

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/24145932

Abstract