Genealogy and clinical course of catecholaminergic polymorphic ventricular tachycardia caused by the ryanodine receptor type 2 P2328S mutation.

<h4>Background</h4>Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe inherited arrhythmic disease associated with a risk of syncope and sudden cardiac death (SCD).<h4>Aims</h4>We aimed at identifying RYR2 P2328S founder mutation carriers and describing the clinical course asso...

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Main Authors:	Mikael Koponen, Annukka Marjamaa, Annukka M Tuiskula, Matti Viitasalo, Terhi Nallinmaa-Luoto, Jaakko T Leinonen, Elisabeth Widen, Lauri Toivonen, Kimmo Kontula, Heikki Swan
Format:	Artigo
Language:	Inglês
Published:	Public Library of Science (PLoS) 2020-01-01
Series:	PLoS ONE
Online Access:	https://doi.org/10.1371/journal.pone.0243649
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