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Article

[Familial hypobetalipoproteinemia secondary to a mutation in the apolipoprotein B gene].

Anales de pediatria (Barcelona, Spain : 2003) - 1 May 2007

Blanco-Rodríguez M, Muñoz-Calvo M T, Martos-Moreno G A, Abad-Pérez E, Argente-Oliver J

Abstract excerpt

Familial hypobetalipoproteinemia (FHB) is a rare genetically heterogeneous disorder provoking abnormally low serum levels of apoprotein (apo) B, total cholesterol, and low-density lipoprotein (LDL-C). Patients carrying heterozygous mutations in the APOB (2p24) gene are usually asymptomatic, but h...

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Identifiers

PMID: 17517208
DOI: 10.1157/13102518

Genes

APOB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17517208-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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