Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death

AIMS: Catecholaminergic polymorphic ventricular tachycardia (CPVT) and short QT syndrome (SQTS) are inherited arrhythmogenic disorders that can cause sudden death. Numerous genes have been reported to cause these conditions, but evidence supporting these gene–disease relationships varies considerabl...

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Detalles Bibliográficos
Autores principales: Walsh, Roddy, Adler, Arnon, Amin, Ahmad S, Abiusi, Emanuela, Care, Melanie, Bikker, Hennie, Amenta, Simona, Feilotter, Harriet, Nannenberg, Eline A, Mazzarotto, Francesco, Trevisan, Valentina, Garcia, John, Hershberger, Ray E, Perez, Marco V, Sturm, Amy C, Ware, James S, Zareba, Wojciech, Novelli, Valeria, Wilde, Arthur A M, Gollob, Michael H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Translational Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9009401/
https://www.ncbi.nlm.nih.gov/pubmed/34557911
http://dx.doi.org/10.1093/eurheartj/ehab687

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9009401/
https://www.ncbi.nlm.nih.gov/pubmed/34557911
http://dx.doi.org/10.1093/eurheartj/ehab687

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