Clinical utility gene card for: Catecholaminergic polymorphic ventricular tachycardia (CPVT)
- PMID: 23549275
- PMCID: PMC3865399
- DOI: 10.1038/ejhg.2013.55
Clinical utility gene card for: Catecholaminergic polymorphic ventricular tachycardia (CPVT)
References
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- Priori SG, Napolitano C, Tiso N, et al. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Circulation. 2001;103:196–200. - PubMed
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- Venetucci L, Denegri M, Napolitano C, Priori SG. Inherited calcium channelopathies in the pathophysiology of arrhythmias. Nat Rev Cardiol. 2012;9:561–575. - PubMed
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- van der Werf C, Nederend I, Hofman N, et al. Familial evaluation in catecholaminergic polymorphic ventricular tachycardia: disease penetrance and expression in cardiac ryanodine receptor mutation-carrying relatives. Circ Arrhythm Electrophysiol. 2012;5:748–756. - PubMed
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- Hong RA, Rivera KK, Jittirat A, Choi JJ. Flecainide suppresses defibrillator-induced storming in catecholaminergic polymorphic ventricular tachycardia. Pacing Clin Electrophysiol. 2012;35:794–797. - PubMed
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