Referenced in: none

Automatically associated channels: Kir1.1 , Kir6.2

Title: Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations.

Authors: Huseyin Demirbilek, Ved Bhushan Arya, Mehmet Nuri Ozbek, Aysehan Akinci, Murat Dogan, Fatma Demirel, Jayne Houghton, Sultan Kaba, Fatma Guzel, Riza Taner Baran, Sevim Unal, Selahattin Tekkes, Sarah E Flanagan, Sian Ellard, Khalid Hussain

Journal, date & volume: Eur. J. Endocrinol., 2014 Jun , 170, 885-92

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/24686051

Abstract