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Article

Point mutations in lipoprotein lipase (LPL) gene: prevalence in normal and combined hyperlipidemic subjects.

Zeitschrift fur Gastroenterologie - 1 Jun 1996

Gehrisch S, Steinke M, Kostka H, Hoche I, Julius U, Jaross W

Abstract excerpt

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Topics

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Share to Aged
Share to Amino Acid Sequence
Share to Hyperlipidemia, Familial Combined
Share to Lipids

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lipoprotein Lipase

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Share to Point Mutation

Share to Triglycerides

Source

Identifiers

PMID: 8767466

Genes

LPL

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026.

Related research

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Point mutations in lipoprotein lipase (LPL) gene: prevalence in normal and combined hyperlipidemic subjects.PMID 8767466Read ↗

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Dyslipidemias associated with heterozygous lipoprotein lipase mutations in the French-Canadian population.Semantic proximity Read ↗

Study of Common Genetic Variant S447X in Lipoprotein Lipase and Its Association with Lipids and Lipoproteins in Type 2 Diabetic PatientsSemantic proximity Read ↗

Analysis of DNA changes in the LPL gene in patients with familial combined hyperlipidemia.Semantic proximity Read ↗

The lipoprotein lipase (Asn291-->Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia.Semantic proximity Read ↗

Lipoprotein lipase (A1127G) gene polymorphism: a case-control association study.Semantic proximity Read ↗

Ser477Stop mutation of the lipoprotein lipase gene occurs at a higher frequency in Japanese subjects with normal triglyceride levels than in hypertriglyceridemic patients.Semantic proximity Read ↗

[Primary lipoprotein lipase deficiency: clinical and genetic aspects].Semantic proximity Read ↗

Absence of apolipoprotein B3500 mutation in type 2a hyperlipoproteinemia patients and in the general population from southern Italy.Semantic proximity Read ↗

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