2021
DOI: 10.1093/eurheartj/ehab724.0633
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Molecular characterization of a cohort of individuals referred to genetic testing with suspected CPVT

Abstract: Background Catecholaminergic polymorphic ventricular tachycardia (CPVT) is one of the most lethal inherited arrhythmogenic diseases and it mainly affects the young, in the absence of structural heart disease. This condition is difficult to diagnose and the first expression of disease can be an arrhythmic death. In the last years, genetic testing has become a useful tool in the challenging task of CPVT diagnosis. The diagnostic yield of the genetic study is highly variable an… Show more

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