| Literature DB >> 18060996 |
Patrick T Ellinor1, B Alexander Yi, Calum A MacRae.
Abstract
Recent studies of atrial fibrillation (AF) have identified mutations in a series of ion mutations; however, these channels appear to be relatively rare causes of AF. Recent genome-wide association studies for AF have identified novel variants associated with the disease, although the mechanism of action for these variants remains unknown. Ultimately, a greater understanding of the genetics of AF should yield insights into novel pathways, therapeutic targets, and diagnostic testing for this common arrhythmia.Entities:
Mesh:
Year: 2008 PMID: 18060996 PMCID: PMC2905167 DOI: 10.1016/j.mcna.2007.09.005
Source DB: PubMed Journal: Med Clin North Am ISSN: 0025-7125 Impact factor: 5.456