Plakophilin-2 Truncation Variants in Patients Clinically Diagnosed With Catecholaminergic Polymorphic Ventricular Tachycardia and Decedents With Exercise-Associated Autopsy Negative Sudden Unexplained Death in the Young

This study determined if radical plakophilin-2 (PKP2) variants might underlie some cases of clinically diagnosed catecholaminergic polymorphic ventricular tachycardia (CPVT) and exercise-associated, autopsy-negative sudden unexplained death in the young (SUDY). Pathogenic variants in PKP2 cause arrh...

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Veröffentlicht in:	JACC. Clinical electrophysiology 2019-01, Vol.5 (1), p.120-127
Hauptverfasser:	Tester, David J., Ackerman, Jaeger P., Giudicessi, John R., Ackerman, Nicholas C., Cerrone, Marina, Delmar, Mario, Ackerman, Michael J.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult arrhythmogenic right ventricular cardiomyopathy catecholaminergic genetic testing Child Death, Sudden, Cardiac - epidemiology DNA Mutational Analysis Exercise Female Genetic Predisposition to Disease - epidemiology Genetic Predisposition to Disease - genetics Humans Male plakophilin-2 Plakophilins - genetics polymorphic ventricular tachycardia sudden unexplained death in the young Tachycardia, Ventricular - epidemiology Tachycardia, Ventricular - genetics Young Adult
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