Human ether-à-go-go-related gene mutation L539fs/47-hERG leads to cell apoptosis through the endoplasmic reticulum stress pathway

Congenital long QT syndrome (LQTS) is a cardiac channelopathy that often results in fatal arrhythmias. LQTS mutations not only lead to abnormal myocardial electrical activities but are associated with heart contraction abnormalities, cardiomyopathy and congenital heart defects. In vivo and in vitro...

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Detalles Bibliográficos
Autores principales: Ma, Shuting, Zhao, Yun, Cao, Miaomiao, Sun, Chaofeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365044/
https://www.ncbi.nlm.nih.gov/pubmed/30628647
http://dx.doi.org/10.3892/ijmm.2019.4049

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6365044/
https://www.ncbi.nlm.nih.gov/pubmed/30628647
http://dx.doi.org/10.3892/ijmm.2019.4049

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