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Article

The 9p21.3 locus and cardiovascular risk in familial hypercholesterolemia.

Journal of clinical lipidology - 1 Jan 2000

Paquette Martine, Chong Michael, Saavedra Yascara Grisel Luna, Paré Guillaume, Dufour Robert, Baass Alexis

Abstract excerpt

BACKGROUND: Carrying a risk variant in the 9p21.3 locus represents one of the strongest genetic risk factors for atherosclerotic cardiovascular disease (ASCVD) in the general population. However, the effect of these polymorphisms in patients with familial hypercholesterolemia (FH) has never been studied. OBJECTIVE: The objective of this study was to investigate the association between the sentinel 9p21.3 single...

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Share to Chromosomes, Human, Pair 9

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 28502497
DOI: 10.1016/j.jacl.2017.01.012

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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