Autopsy and postmortem examination case study on genetic risk factors for cardiac death: Polymorphisms of endothelial nitric oxide synthase gene Glu298asp variant and T-786c mutation, human paraoxonas

Autopsy and postmortem examination case study on genetic risk factors for cardiac death: Polymorphisms of endothelial nitric oxide synthase gene Glu298asp variant and T-786c mutation, human paraoxonas

Background/Aim. The Glu298Asp variant in exon 7 and T-786C mutation in the 5'-flanking region of the endothelial nitric oxide synthase (eNOS) gene, paraoxonase I gene (PON1), and α2β- adrenergic receptor gene (α2β-AR) have been reported to be genetic risk factors for coronary heart disease (CHD...

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Bibliographic Details
Main Authors: Ameno Kiyoshi, Ameno Setsuko, Kinoshita Hiroshi, Jamal Mostofa, Wang Weihuan, Kumihashi Mitsuru, Uekita Ikuo, Ijiri Iwao
Format: Article
Language:English
Published: Ministry of Defence of the Republic of Serbia, University of Defence, Belgrade 2006-01-01
Series:Vojnosanitetski Pregled
Subjects:
forensic medicine
death
sudden
cardiac
coronarydisease
risk factors
polymorphism
genetic
Online Access:http://www.doiserbia.nb.rs/img/doi/0042-8450/2006/0042-84500604357A.pdf
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http://www.doiserbia.nb.rs/img/doi/0042-8450/2006/0042-84500604357A.pdf

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