Modeling Tissue- and Mutation- Specific Electrophysiological Effects in the Long QT Syndrome: Role of the Purkinje Fiber

Congenital long QT syndrome is a heritable family of arrhythmias caused by mutations in 13 genes encoding ion channel complex proteins. Mounting evidence has implicated the Purkinje fiber network in the genesis of ventricular arrhythmias. In this study, we explore the hypothesis that long QT mutatio...

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Detalles Bibliográficos
Autores principales: Iyer, Vivek, Sampson, Kevin J., Kass, Robert S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4043730/
https://www.ncbi.nlm.nih.gov/pubmed/24892747
http://dx.doi.org/10.1371/journal.pone.0097720

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4043730/
https://www.ncbi.nlm.nih.gov/pubmed/24892747
http://dx.doi.org/10.1371/journal.pone.0097720

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