Ontology highlight
ABSTRACT:
SUBMITTER: Lubitz SA
PROVIDER: S-EPMC2675914 | biostudies-literature | 2009 Feb
REPOSITORIES: biostudies-literature
Lubitz Steven A SA Yi B Alexander BA Ellinor Patrick T PT
Cardiology clinics 20090201 1
Recent studies of AF have identified mutations in a series of ion channels; however, these mutations appear to be relatively rare causes of AF. A genome-wide association study has identified novel variants on chromosome 4 associated with AF, 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. ...[more]