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Article

Haplotype analyses of the APOA5 gene in patients with familial combined hyperlipidemia.

Biochimica et biophysica acta - 1 Jan 2007

van der Vleuten Gerly M, Isaacs Aaron, Zeng Wu-Wei, ter Avest Ewoud, Talmud Philippa J, Dallinga-Thie Geesje M, van Duijn Cornelia M, Stalenhoef Anton F H, de Graaf Jacqueline

Abstract excerpt

BACKGROUND: Familial combined hyperlipidemia (FCH) is the most common genetic lipid disorder with an undefined genetic etiology. Apolipoprotein A5 gene (APOA5) variants were previously shown to contribute to FCH. The aim of the present study was to evaluate the association of APOA5 variants with FCH and its related phenotypes in Dutch FCH patients. Furthermore, the effects of variants in the APOA5 gene on carotid...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17157483
DOI: 10.1016/j.bbadis.2006.10.012

Genes

APOA5

Variants

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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