Cardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope.
- Author:
Ngai-Shing MOK
1
;
Ching-Wan LAM
;
Nai-Chung FONG
;
Yim-Wo HUI
;
Yuen-Choi CHOI
;
Kwok-Yin CHAN
Author Information
1. Department of Medicine & Geriatrics, Princess Margaret Hospital, Hong Kong, China. isaacmok@netvigator.com
- Publication Type:Case Reports
- MeSH:
Adolescent;
Death, Sudden, Cardiac;
etiology;
Female;
Humans;
Ion Channels;
physiology;
Mutation;
Ryanodine Receptor Calcium Release Channel;
genetics;
Syncope;
etiology;
Tachycardia, Ventricular;
genetics
- From:
Chinese Medical Journal
2006;119(24):2129-2133
- CountryChina
- Language:English
