Referenced in: none

Automatically associated channels: Kv2.1

Title: Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism.

Authors: C Saint-Martin, Q Zhou, G M Martin, C Vaury, G Leroy, J-B Arnoux, P de Lonlay, S-L Shyng, C Bellanne-Chantelot

Journal, date & volume: Clin. Genet., 2015 May , 87, 448-54

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/24814349

Abstract