𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Mutation analysis of KCNQ1, KCNH2, SCN5A, KCNE1 and KCNE2 genes in Chinese patients with long QT syndrome

✍ Scribed by Du, Rong ;Tian, Li ;Yuan, Guohui ;Li, Jin ;Ren, Faxin ;Gui, Le ;Li, Wei ;Zhang, Shouyan ;Kang, Cailian ;Yang, Junguo


Book ID
107472162
Publisher
Higher Education Press and Springer
Year
2007
Tongue
English
Weight
460 KB
Volume
1
Category
Article
ISSN
1673-7342

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


KCNQ1 and KCNH2 mutations associated wit
✍ Wenling Liu; Junguo Yang; Dayi Hu; Cailian Kang; Cuilan Li; Shuoyan Zhang; Ping πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 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