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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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Библиографические подробности
Опубликовано в: :Int J Med Sci
Главные авторы: 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
Формат: Artigo
Язык:Inglês
Опубликовано: Ivyspring International Publisher 2018
Предметы:
Online-ссылка: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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