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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...

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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

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