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Article

Contribution of chromosome 1q21-q23 to familial combined hyperlipidemia in Mexican families.

Annals of human genetics - 1 Sept 2004

Huertas-Vázquez A, del Rincón J P, Canizales-Quinteros S, Riba L, Vega-Hernández G, Ramírez-Jiménez S, Aurón-Gómez M, Gómez-Pérez F J, Aguilar-Salinas C A, Tusié-Luna M T

Abstract excerpt

Familial combined hyperlipidemia (FCHL) is the most common familial dyslipidemia, with a prevalence of 1-2% in the general population. A major locus for FCHL has been mapped to chromosome 1q21-q23 in Finnish, Chinese, German and US families. We studied seven extended Mexican families with 153 mem...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15469419
DOI: 10.1046/j.1529-8817.2003.00116.x

Genes

APOA1
LCAT
LIPC
LPL
NPL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-15469419-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

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

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