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Cellular Mechanisms of Sinus Node Dysfunction in Carriers of the SCN5A-E161K Mutation and Role of the H558R Polymorphism

Background: Carriers of the E161K mutation in the SCN5A gene, encoding the Na(V)1.5 pore-forming α-subunit of the ion channel carrying the fast sodium current (I(Na)), show sinus bradycardia and occasional exit block. Voltage clamp experiments in mammalian expression systems revealed a mutation-indu...

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Detalles Bibliográficos
Autor principal: Wilders, Ronald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305593/
https://www.ncbi.nlm.nih.gov/pubmed/30618807
http://dx.doi.org/10.3389/fphys.2018.01795