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Article

A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.

American journal of human genetics - 1 Aug 1999

Aouizerat B E, Allayee H, Cantor R M, Davis R C, Lanning C D, Wen P Z, Dallinga-Thie G M, de Bruin T W, Rotter J I, Lusis A J

Abstract excerpt

Familial combined hyperlipidemia (FCHL) is a common familial lipid disorder characterized by a variable pattern of elevated levels of plasma cholesterol and/or triglycerides. It is present in 10%-20% of patients with premature coronary heart disease. The genetic etiology of the disease, including...

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Share to Chromosomes, Human, Pair 11
Share to Hyperlipidemia, Familial Combined

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Multifactorial Inheritance

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Source

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Identifiers

PMID: 10417282
DOI: 10.1086/302490
PMCID: PMC1377938

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-10417282-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

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