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Article

Analysis of apolipoprotein A-I, lecithin:cholesterol acyltransferase and glucocerebrosidase genes in hypoalphalipoproteinemia.

Atherosclerosis - 1 Jul 2002

Recalde Delia, Cenarro Ana, García-Otín Angel-Luis, Gómez-Coronado Diego, Civeira Fernando, Pocoví Miguel

Abstract excerpt

Hypoalphalipoproteinemia (HALP) is a dyslipidemia characterized by low HDL-cholesterol (HDL-C) levels with important genetic contribution. However, no common genetic mutations have been found to be associated with this disorder. We screened the promoter and coding sequence of apolipoprotein (apo) A-I and lecithin:cholesterol acyltransferase (LCAT) genes and the 5' apo C-III region by SSCP and heteroduplex...

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Share to Analysis of Variance
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Glucosylceramidase

Share to Phosphatidylcholine-Sterol O-Acyltransferase

Share to Polymerase Chain Reaction

Share to Polymorphism, Genetic

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Source

Identifiers

PMID: 12048121
DOI: 10.1016/s0021-9150(01)00753-5

Genes

LCAT

Variants

Provenance

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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