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Article

[Mutations of the lamin A/C gene causing familial partial lipodystrophy: significance for the development of hyperlipidemia and insulin resistant diabetes mellitus].

Zeitschrift fur Gastroenterologie - 1 Apr 2000

Genschel J, Lochs H, Schmidt H H

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Topics

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Share to Amino Acid Substitution
Share to Chromosomes, Human, Pair 1
Share to Diabetes Mellitus, Type 2
Share to Hyperlipidemias

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Insulin Resistance

Share to Lamin Type A

Share to Lamins

Share to Lipodystrophy

Source

Identifiers

PMID: 10820868

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Mutations of the lamin A/C gene causing familial partial lipodystrophy: significance for the development of hyperlipidemia and insulin resistant diabetes mellitus].PMID 10820868Read ↗

Familial partial lipodystrophy associated with the heterozygous LMNA mutation 1445G>A (Arg482Gln) in a Polish family.Semantic proximity Read ↗

[Laminopathies: lipodystrophies, insulin resistance, syndromes of accelerated ageing... and others].Semantic proximity Read ↗

Association between nuclear lamin A/C R482Q mutation and partial lipodystrophy with hyperinsulinemia, dyslipidemia, hypertension, and diabetes.Semantic proximity Read ↗

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[Genetic basis for dyslipidemias].Semantic proximity Read ↗

[Gene mutations responsible for hyperlipoproteinemia].Semantic proximity Read ↗

Navigating Lipodystrophy: Insights from Laminopathies and Beyond.Semantic proximity Read ↗

Lipodystrophy: beyond generalization?Semantic proximity Read ↗

Adipokines and the insulin resistance syndrome in familial partial lipodystrophy caused by a mutation in lamin A/C.Semantic proximity Read ↗

[Gene mutations in familial hyperlipidemias].Semantic proximity Read ↗

Familial partial lipodystrophy syndromes.Semantic proximity Read ↗

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