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

Article ID	Journal	Published Year	Pages	File Type
2922430	Heart Rhythm	2013	4 Pages	PDF

Keywords

SCN5A LQTS QTc KCNH2 KCNE1 QTcB Per-Arnt-Sim ECG electrocardiogram Long QT syndrome Molecular screening corrected QT interval PAS

Related Topics

Health Sciences Medicine and Dentistry Cardiology and Cardiovascular Medicine

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

Authors

Yukako MD, Masao MD, PhD, Kunihiro MD, PhD, Shinichi MD, PhD,