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Article

Donor splice-site mutation (210+1G_C) in the ApoB gene causes a very low level of ApoB-100 and LDL cholesterol.

Arteriosclerosis, thrombosis, and vascular biology - 1 Nov 2001

Welty F K, Guida K A, Andersen J J

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Share to Apolipoprotein B-100
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Share to Cholesterol, LDL

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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PMID: 11701479

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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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Donor splice-site mutation (210+1G_C) in the ApoB gene causes a very low level of ApoB-100 and LDL cholesterol.PMID 11701479Read ↗

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Familial defective apolipoprotein B-100: molecular basis, prevalence and clinical features.Semantic proximity Read ↗

Donor splice mutation (665 + 1 G_T) in familial hypobetalipoproteinemia with no detectable apoB truncation.Semantic proximity Read ↗

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

Rare Protein-Truncating Variants in APOB , Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart DiseaseSemantic proximity Read ↗

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Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia.Semantic proximity Read ↗

H3543Y mutation of apoB-100 in patients with phenotype of familial hypercholesterolemia.Semantic proximity Read ↗

Novel APOB mutation in familial hypobetalipoproteinemia.Semantic proximity Read ↗

Mutations and variants of apolipoprotein B that affect plasma cholesterol levels.Semantic proximity Read ↗

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