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Article

Association of USF1 and APOA5 polymorphisms with familial combined hyperlipidemia in an Italian population.

Molecular and cellular probes - 1 Feb 2015

Di Taranto Maria Donata, Staiano Antonino, D'Agostino Maria Nicoletta, D'Angelo Antonietta, Bloise Elena, Morgante Alberto, Marotta Gennaro, Gentile Marco, Rubba Paolo, Fortunato Giuliana

Abstract excerpt

BACKGROUND: Familial combined hyperlipidemia (FCH) is a polygenic and multifactorial disease characterized by a variable phenotype showing increased levels of triglycerides and/or cholesterol. The aim of this study was to identify single nucleotides (SNPs) in lipid-related genes associated with FCH. METHODS AND RESULTS: Twenty SNPs in lipid-related genes were studied in 142 control subjects and 165 FCH patients...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 25308402
DOI: 10.1016/j.mcp.2014.10.002

Genes

APOA5
APOE
LDLR

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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