CASQ2 variants in Chinese children with catecholaminergic polymorphic ventricular tachycardia

CASQ2 variants in Chinese children with catecholaminergic polymorphic ventricular tachycardia

Abstract Background Biallelic variants of the CASQ2 are known to cause the autosomal recessive form of catecholaminergic polymorphic ventricular tachycardia (CPVT), an inherited disease that predisposes young individuals to syncope and sudden cardiac death. To date, only about 24 CASQ2 variants have...

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Bibliographic Details
Main Authors: Qirui Li, Ruolan Guo, Lu Gao, Lang Cui, Zhihui Zhao, Xia Yu, Yue Yuan, Xiwei Xu
Format: Article
Language:English
Published: Wiley 2019-11-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
autosomal recessive
CASQ2 variants
catecholaminergic polymorphic ventricular tachycardia
targeted next‐generation sequencing
Online Access:https://doi.org/10.1002/mgg3.949

Internet

https://doi.org/10.1002/mgg3.949

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