A novel mutation (Arg169Gln) of the cardiac ryanodine receptor gene causing exercise-induced bidirectional ventricular tachycardia
Authors:
- Chia-Hsiang HsuehCHChia-Hsiang Hsueh
- Yi-Chun WengYWYi-Chun Weng
- Chao-Yu ChenCCChao-Yu Chen
- Tin-Kwang LinTLTin-Kwang Lin
- Yen-Hung LinYLYen-Hung Lin
- Ling-Ping LaiLLLing-Ping Lai
- Jiunn-Lee LinJLJiunn-Lee Lin
- 1 April 2006
- journal article
- research article
- Published by Elsevier in International Journal of Cardiology
- Vol. 108 (2) , 276-278
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardiaJournal of Cellular Physiology, 2001
- Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)Human Molecular Genetics, 2001
- Mutations in the Cardiac Ryanodine Receptor Gene ( hRyR2 ) Underlie Catecholaminergic Polymorphic Ventricular TachycardiaCirculation, 2001
- Ryanodine receptor isoforms in excitation-contraction couplingAdvances in Biophysics, 1999
- The human cardiac muscle ryanodine receptor-calcium release channel: identification, primary structure and topological analysisBiochemical Journal, 1996
- Catecholaminergic Polymorphic Ventricular Tachycardia in ChildrenCirculation, 1995