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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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| Udgivet i: | Int J Med Sci |
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| Main Authors: | , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Ivyspring International Publisher
2018
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| Fag: | |
| Online adgang: | 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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