قاسمی, شیرین

[ 1 ] - مقایسه پلی‌مورفیسم rs5186 (A1166C)ژن AGTR1 بیماران ایرانی مبتلا به عروق کرونری با افراد سالم: یک مطالعه مورد- شاهدی

Background and Aim: Coronary artery disease (CAD) is a multifactorial inherited disorder in which the arteries that blood to the heart muscle become hardened and narrowed. We aimed at investigating the role of rs5186 (A1166C) polymorphism the angiotensin II type 1 receptor (AGTR1) gene as risk factors in some Iranian CAD patients. Materials and Methods: In this case-control study 137 samples...