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Article

Novel genes for familial combined hyperlipidemia.

Current opinion in lipidology - 1 Apr 1999

Aouizerat B E, Allayee H, Bodnar J, Krass K L, Peltonen L, de Bruin T W, Rotter J I, Lusis A J

Abstract excerpt

Familial combined hyperlipidemia (FCHL) is a complex genetic disorder of unknown etiology. Recently, 'modifier' genes of the FCHL phenotype, such as the apolipoprotein AI-CIII-AIV gene cluster and LPL, have been identified in several populations. A 'major' gene for FCHL has been identified in a Finnish isolate which maps to a region syntenic to murine chromosome 3 where a locus for combined hyperlipidemia has...

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Source

Identifiers

PMID: 10327279
DOI: 10.1097/00041433-199904000-00005

Genes

LPL

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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