Referenced in: Kv11.1

Automatically associated channels: Kir2.3 , Kir6.2 , Kv11.1

Title: Recurrent intrauterine fetal loss due to near absence of HERG: clinical and functional characterization of a homozygous nonsense HERG Q1070X mutation.

Authors: Zahurul A Bhuiyan, Tarek S Momenah, Qiuming Gong, Ahmad S Amin, Saleh Al Ghamdi, Julene S Carvalho, Tessa Homfray, Marcel M A M Mannens, Zhengfeng Zhou, Arthur A M Wilde

Journal, date & volume: Heart Rhythm, 2008 Apr , 5, 553-61

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/18362022

Abstract