Arrhythmogenic mechanism of a novel ryanodine receptor mutation underlying sudden cardiac death

AIMS: The ryanodine receptor 2 (RyR2) is essential for cardiac muscle excitation–contraction coupling; dysfunctional RyR2 participates in the development of inherited arrhythmogenic cardiac disease. In this study, a novel RyR2 mutation A690E is identified from a patient with family inheritance of su...

Descripción completa

Detalles Bibliográficos
Autores principales: Qian, Yunyun, Zuo, Dongchuan, Xiong, Jing, Yin, Yihen, Qi, Ruxi, Ma, Xiaomin, Yan, An, Yang, Yawen, Liu, Ping, Zhang, Jingying, Tang, Kai, Peng, Wenhui, Xu, Yawei, Liu, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Translational Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374982/
https://www.ncbi.nlm.nih.gov/pubmed/37466361
http://dx.doi.org/10.1093/europace/euad220

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374982/
https://www.ncbi.nlm.nih.gov/pubmed/37466361
http://dx.doi.org/10.1093/europace/euad220

Ejemplares similares