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Article

Novel APOB mutation in familial hypobetalipoproteinemia.

Journal of clinical lipidology - 1 Jan 2000

Domenech M, Llano-Rivas Isabel, Arroyo Vicente, Ortega Emilio

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Identifiers

PMID: 34852964
DOI: 10.1016/j.jacl.2021.11.003

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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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Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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Novel APOB mutation in familial hypobetalipoproteinemia.PMID 34852964Read ↗

Novel human pathological mutations. Gene symbol: APOB. Disease: normotriglyceridemic hypobetalipoproteinemia.Semantic proximity Read ↗

Novel mutation (c.G1124A) in exon 9 of the APOB gene causes aberrant splicing and familial hypobetalipoproteinemia.Semantic proximity Read ↗

A novel mutation of apolipoprotein B in a French Canadian family with homozygous hypobetalipoproteinemia.Semantic proximity Read ↗

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Lipid disorders and mutations in the APOB gene.Semantic proximity Read ↗

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High frequency of APOB gene mutations causing familial hypobetalipoproteinaemia in patients of Dutch and Spanish descent.Semantic proximity Read ↗

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[Familial hypobetalipoproteinemia].Semantic proximity Read ↗

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