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Article

Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol acyltransferase on 16q.

Arteriosclerosis, thrombosis, and vascular biology - 1 Nov 1999

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

Abstract excerpt

Familial combined hyperlipidemia (FCHL) is a common lipid disorder characterized by elevated levels of plasma cholesterol and triglycerides that is present in 10% to 20% of patients with premature coronary artery disease. To study the pathophysiological basis and genetics of FCHL, we previously reported recruitment of 18 large families. We now report linkage studies of 14 candidate genes selected for their...

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Source

Identifiers

PMID: 10559018
DOI: 10.1161/01.atv.19.11.2730

Genes

LCAT

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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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