A SHOX2 loss-of-function mutation underlying familial atrial fibrillation

Atrial fibrillation (AF), as the most common sustained cardiac arrhythmia, is associated with substantially increased morbidity and mortality. Aggregating evidence demonstrates that genetic defects play a crucial role in the pathogenesis of AF, especially in familial AF. Nevertheless, AF is of prono...

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Detalhes bibliográficos
Publicado no:Int J Med Sci
Main Authors: Li, Ning, Wang, Zhang-Sheng, Wang, Xin-Hua, Xu, Ying-Jia, Qiao, Qi, Li, Xiu-Mei, Di, Ruo-Min, Guo, Xiao-Juan, Li, Ruo-Gu, Zhang, Min, Qiu, Xing-Biao, Yang, Yi-Qing
Formato: Artigo
Idioma:Inglês
Publicado em: Ivyspring International Publisher 2018
Assuntos:
Research Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6216059/
https://ncbi.nlm.nih.gov/pubmed/30443179
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7150/ijms.27424
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