A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia

BACKGROUND: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a lethal inherited arrhythmia syndrome characterized by adrenergically stimulated ventricular tachycardia. Mutations in the cardiac ryanodine receptor gene (RYR2) cause an autosomal dominant form of CPVT, while mutations in...

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Publicado no:Heart Rhythm
Main Authors: Gray, Belinda, Bagnall, Richard D., Lam, Lien, Ingles, Jodie, Turner, Christian, Haan, Eric, Davis, Andrew, Yang, Pei-Chi, Clancy, Colleen E., Sy, Raymond W., Semsarian, Christopher
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5453511/
https://ncbi.nlm.nih.gov/pubmed/27157848
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2016.05.004
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