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...
Main Authors: | , , , |
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Format: | Article |
Language: | fas |
Published: |
Birjand University of Medical Sciences and Health Services
2017-05-01
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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 |