Genetic and clinical characteristics of catecholaminergic polymorphic ventricular tachycardia in a Taiwanese nationwide cohort

Background: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare and lethal arrhythmia. Ryanodine receptor 2 (RYR2) mutation accounts for ∼60% of CPVT patients which is inherited in an autosomal dominant pattern. Objective: This study aimed to identify CPVT-related mutations and cl...

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Hlavní autoři:	Grace Chia-Yen Hsu, Mei-Hwan Wu, Jing-Yuan Chuang, Shuenn-Nan Chiu, Ming-Tai Lin, Ling-Ping Lai, Shih-Fan Sherri Yeh, Sheng-Fu Liu, Ting-Tse Lin, Fu-Tien Chiang, Jyh-Ming Jimmy Juang
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	Elsevier 2025-08-01
Edice:	Journal of the Formosan Medical Association
Témata:	Catecholaminergic polymorphic ventricular tachycardia (CPVT) Ventricular arrhythmia Inheritable arrhythmia Sudden cardiac death Population genetics and genomics
On-line přístup:	http://www.sciencedirect.com/science/article/pii/S0929664624003413
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