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

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...

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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: Article
Language:English
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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https://doi.org/10.1371/journal.pone.0243649

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