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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Guardat en:
Dades bibliogràfiques
Publicat a:Int J Med Sci
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Ivyspring International Publisher 2018
Matèries:
Research Paper
Accés en línia: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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