A novel mutation in the SCN5A gene contributes to arrhythmogenic characteristics of early repolarization syndrome

Several genetic variants have been associated with early repolarization syndrome (ERS). However, the lack of functional validations of the mutant effects has limited the interpretation of genetic tests. In the present study, we identified and characterized a novel sodium channel, voltage gated, type...

Descripción completa

Detalles Bibliográficos
Autores principales: GUO, QI, REN, LAN, CHEN, XUHUA, HOU, CUIHONG, CHU, JIANMIN, PU, JIELIN, ZHANG, SHU
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4771109/
https://www.ncbi.nlm.nih.gov/pubmed/26820605
http://dx.doi.org/10.3892/ijmm.2016.2468

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4771109/
https://www.ncbi.nlm.nih.gov/pubmed/26820605
http://dx.doi.org/10.3892/ijmm.2016.2468

Ejemplares similares