PRRX1 Loss‐of‐Function Mutations Underlying Familial Atrial Fibrillation

BACKGROUND: Atrial fibrillation (AF) is the most common form of clinical cardiac dysrhythmia responsible for thromboembolic cerebral stroke, congestive heart failure, and death. Aggregating evidence highlights the strong genetic basis of AF. Nevertheless, AF is of pronounced genetic heterogeneity, a...

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Detalles Bibliográficos
Autores principales: Guo, Xiao‐Juan, Qiu, Xing‐Biao, Wang, Jun, Guo, Yu‐Han, Yang, Chen‐Xi, Li, Li, Gao, Ri‐Feng, Ke, Zun‐Ping, Di, Ruo‐Min, Sun, Yu‐Min, Xu, Ying‐Jia, Yang, Yi‐Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075371/
https://www.ncbi.nlm.nih.gov/pubmed/34845933
http://dx.doi.org/10.1161/JAHA.121.023517

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9075371/
https://www.ncbi.nlm.nih.gov/pubmed/34845933
http://dx.doi.org/10.1161/JAHA.121.023517

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