Referenced in: none

Automatically associated channels: Kv11.1 , Nav1.5

Title: A case of long QT syndrome with triple gene abnormalities: digenic mutations in KCNH2 and SCN5A and gene variant in KCNE1.

Authors: Yukako Yoshikane, Masao Yoshinaga, Kunihiro Hamamoto, Shinichi Hirose

Journal, date & volume: Heart Rhythm, 2013 Apr , 10, 600-3

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/23237912

Abstract