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

BACKGROUND: Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe inherited arrhythmic disease associated with a risk of syncope and sudden cardiac death (SCD). AIMS: We aimed at identifying RYR2 P2328S founder mutation carriers and describing the clinical course associated with t...

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Detalles Bibliográficos
Autores principales: Koponen, Mikael, Marjamaa, Annukka, Tuiskula, Annukka M., Viitasalo, Matti, Nallinmaa-Luoto, Terhi, Leinonen, Jaakko T., Widen, Elisabeth, Toivonen, Lauri, Kontula, Kimmo, Swan, Heikki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735638/
https://www.ncbi.nlm.nih.gov/pubmed/33315912
http://dx.doi.org/10.1371/journal.pone.0243649

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735638/
https://www.ncbi.nlm.nih.gov/pubmed/33315912
http://dx.doi.org/10.1371/journal.pone.0243649

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