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Article

Genetic copy number variants in myocardial infarction patients with hyperlipidemia.

BMC genomics - 30 Nov 2011

Shia Wei-Chung, Ku Tien-Hsiung, Tsao Yu-Ming, Hsia Chien-Hsun, Chang Yung-Ming, Huang Ching-Hui, Chung Yeh-Ching, Hsu Shih-Lan, Liang Kae-Woei, Hsu Fang-Rong

Abstract excerpt

BACKGROUND: Cardiovascular disease is the chief cause of death in Taiwan and many countries, of which myocardial infarction (MI) is the most serious condition. Hyperlipidemia appears to be a significant cause of myocardial infarction, because it causes atherosclerosis directly. In recent years, copy number variation (CNV) has been analyzed in genomewide association studies of complex diseases. In this study, CNV...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 22369086
DOI: 10.1186/1471-2164-12-S3-S23
PMCID: PMC3333183

Genes

CDC73
CDCP1
CDH13
DISC1
RET

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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