Comparison of AGTR1 rs5186 (A1166C) Polymorphism between Coronary Artery Disease Patients and Normal Subjects: a Case Control Study

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 facto...

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Bibliographic Details
Main Authors: Mohammad Mehdi Heidari, shirin Ghasemi, Faeghe Haji hosseini, Mehdi Hadadzadeh
Format: Article
Language:fas
Published: Birjand University of Medical Sciences and Health Services 2017-05-01
Series:مجله دانشگاه علوم پزشکی بیرجند
Subjects:
Online Access:http://journal.bums.ac.ir/browse.php?a_code=A-10-1521-2&slc_lang=en&sid=1