๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

A case of long QT syndrome having compound mutations of KCNH2 and SCN5A

โœ Scribed by Saki Ito; Takeshi Taketani; Takashi Sugamori; Taiji Okada; Hirotomo Sato; Tomoko Adachi; Masaki Takeda; Nobuhiro Kodani; Nobuyuki Takahashi; Akihiro Endo; Hiroyuki Yoshitomi; Kazuaki Tanabe; Wataru Shimizu


Book ID
118474562
Publisher
Elsevier
Year
2012
Tongue
English
Weight
549 KB
Volume
6
Category
Article
ISSN
1878-5409

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


KCNQ1 and KCNH2 mutations associated wit
โœ Wenling Liu; Junguo Yang; Dayi Hu; Cailian Kang; Cuilan Li; Shuoyan Zhang; Ping ๐Ÿ“‚ Article ๐Ÿ“… 2002 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 285 KB

The long QT syndrome (LQTS) is a cardiac disorder characterized by prolongation of the QT interval on electrocardiograms (ECGs), syncope and sudden death caused by a specific ventricular tachyarrhythmia known as torsade de pointes. LQTS is caused by mutations in ion channel genes including the cardi