Common variant of 5,10-methylenetetrahydrofolate reductase may increase risk of coronary artery disease in the Iranian population

Autor: Seyedpayam Shirangi, Majid Shahbazi, Farnoosh shateri, Marzieh Attar

Publikováno v: Egyptian Journal of Medical Human Genetics, Vol 19, Iss 1, Pp 1-5 (2018)
Egyptian Journal of Medical Human Genetics; Vol 19, No 1 (2018); 1–5

Background Coronary artery disease (CAD) is the most prevalent form of cardiovascular disease that is caused by the formation of plaque in the arteries walls. Both genetic and environmental factors play an important role in the development of CAD. Ai

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8c060e3b02e898b1f3c9bcbbed6fb0f
http://www.sciencedirect.com/science/article/pii/S1110863017301167