Lack of Association between the MEF2A Gene and Coronary Artery Disease in Iranian Families

Objective(s):  Coronary artery disease (CAD) which may lead to myocardial infarction (MI) is a complex one. Great effort has been devoted to identification of genes that increase susceptibility to CAD or provide protection. A 21-bp deletion in the MEF2A gene, which encodes a member of the myocyte en...

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Bibliographic Details
Main Authors: Kolsoum Inanloo Rahatloo, Saeid Davaran, Elahe Elahi
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2013-08-01
Series:Iranian Journal of Basic Medical Sciences
Subjects:
Online Access:http://ijbms.mums.ac.ir/pdf_1356_e32aec158cc726d76de441e93a0bdf0e.html