Increased Risk of the APOB rs11279109 Polymorphism for CHD among the Kuwaiti Population.

Suzanne A Al-BustanFatma G IsmaelAhmad Al-SerriIbrahim Al-Rashdan

Published in: Disease markers (2017)

The DD genotype may explain molecular mechanisms that underline increased LDL oxidation leading to arthrosclerosis. The findings emphasize the need to identify genetic markers specific to the CHD patient ethnic group in order to improve prognosis and help in early diagnosis and prevention.

Keyphrases

case report
genome wide
hydrogen peroxide
copy number
gene expression
dna methylation
low density lipoprotein
nitric oxide
visible light