Article
Joint effect of G1691A factor V point mutation and factor VII Arg/Gln(353) gene polymorphism on the risk of premature coronary artery disease.
Annales de genetique - 1 Jan 2000
Petrovic D, Zorc M, Keber I, Peterlin B
Abstract excerpt
The study sought an association between the G1691A factor V point mutation and factor VII Arg/Gln(353) gene polymorphism and premature coronary artery disease (CAD), and the interactive effect on CAD risk between the G1691A factor V point mutation and factor VII Arg/Gln(353) gene polymorphism as well as between tested polymorphisms and traditional risk factors. 167 patients with CAD younger than 55 years were...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.