A gain of function ryanodine receptor 2 mutation (R1760W-RyR2) in catecholaminergic polymorphic ventricular tachycardia

Li, SY; Lv, TT; Yang, J; Li, K; Yang, Y; Zhang, P

Zhang, P (通讯作者)，Tsinghua Univ, Beijing Tsinghua Changgung Hosp, Sch Clin Med, Dept Cardiol, 168 Litang Rd, Beijing 102218, Peoples R China.

CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2023; 50 (1): 39

Abstract

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited arrhythmia syndrome associated with Ca2+ leak predominantly caused by rya......

Full Text Link


Links

期刊讨论 | 中国SCI论文 | 期刊主页 | 投稿经验 | 杂志官网 | 投稿链接 | 作者需知 | PMC链接 | Pubmed全文检索