Referenced in: none

Automatically associated channels: Kir1.1 , Kir6.2

Title: Clinical and genetic evaluation of patients with KATP channel mutations from the German registry for congenital hyperinsulinism.

Authors: Klaus Mohnike, Ilse Wieland, Winfried Barthlen, Silke Vogelgesang, Susann Empting, Wolfgang Mohnike, Thomas Meissner, Martin Zenker

Journal, date & volume: Horm Res Paediatr, 2014 , 81, 156-68

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/24401662

Abstract