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Article

Functional genetic variants within the SIRT2 gene promoter in acute myocardial infarction.

PloS one - 1 Jan 2017

Yang Wentao, Gao Feng, Zhang Pei, Pang Shuchao, Cui Yinghua, Liu Lixin, Wei Guanghe, Yan Bo

Abstract excerpt

Coronary artery disease (CAD), including acute myocardial infarction (AMI) is the complication of atherosclerosis. Recently, genome-wide association studies have identified a large number of CAD-related genetic variants. However, only 10% of CAD cases could be explained. Low frequent and rare genetic variants have been recently proposed to be main causes for CAD. SIRT2 is a member of sirtuin family,...

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Source

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Identifiers

PMID: 28445509
DOI: 10.1371/journal.pone.0176245
PMCID: PMC5406008

Genes

SIRT2
CAD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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