Open AccessCardiac ryanodine receptor gene (hRyR2) mutation underlying catecholaminergic polymorphic ventricular tachycardia in a Chinese adolescent presenting with sudden cardiac arrest and cardiac syncope
Author(s) -
NgaiShing Mok,
ChingWan Lam,
Nai-Chung Fong,
Yim-Wo Hui,
Yuen-Choi Choi,
Kwok-Yin Chan
Publication year - 2006
Publication title -
chinese medical journal/chinese medical journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.537
H-Index - 63
eISSN - 2542-5641
pISSN - 0366-6999
DOI - 10.1097/00029330-200612020-00018
Subject(s) - catecholaminergic polymorphic ventricular tachycardia , ryanodine receptor 2 , ryanodine receptor , sudden cardiac death , cardiology , medicine , sudden cardiac arrest , ventricular tachycardia , long qt syndrome , ventricular fibrillation , syncope (phonology) , qt interval , receptor