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Article

Apolipoprotein B Arg3500Gln mutation prevalence in children with hypercholesterolemia: a French multicenter study.

Journal of pediatric gastroenterology and nutrition - 1 Aug 2001

Viola S, Benlian P, Morali A, Dobbelaere D, Lacaille F, Rieu D, Ginies J L, Maurage C, Meyer M, Lachaux A, Larchet M, Lenearts C, Goulet O, Sarles J, Mouterde O, Girardet J P

Abstract excerpt

BACKGROUND: Familial defective apolipoprotein B-100, a dominantly inherited form of hypercholesterolemia caused by a single Arg3500Gln mutation, is silent in childhood but may confer a high risk of cardiovascular disease in adulthood. The objective was to determine the prevalence of familial defective apolipoprotein B-100 in hypercholesterolemic French children and to provide a basis for targeting screening...

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Identifiers

PMID: 11568510
DOI: 10.1097/00005176-200108000-00005

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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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