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Article

CAG repeat polymorphism of the MEF2A gene is not associated with the risk of coronary artery disease among Taiwanese.

Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis - 1 Jun 2010

Hsu Lung-An, Chang Chi-Jen, Teng Ming-Sheng, Semon Wu, Hu Chiao-Feng, Chang Wen-Ya, Ko Yu-Lin

Abstract excerpt

A 21-bp deletion mutation of the exon 11 of the myocyte enhancer factor-2A (MEF2A) gene was shown to cause familial coronary artery disease. This finding raises the possibility that MEF2A variants may contribute to the risk of coronary artery disease. In total, 258 patients with coronary artery d...

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Source

Identifiers

PMID: 19153100
DOI: 10.1177/1076029608330476

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19153100-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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CAG repeat polymorphism of the MEF2A gene is not associated with the risk of coronary artery disease among Taiwanese.PMID 19153100Read ↗

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