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Article

Laminopathies and atherosclerosis.

Arteriosclerosis, thrombosis, and vascular biology - 1 Sept 2004

Al-Shali Khalid Z, Hegele Robert A

Abstract excerpt

Laminopathies are genetic diseases that encompass a wide spectrum of phenotypes with diverse tissue pathologies and result mainly from mutations in the LMNA gene encoding nuclear lamin A/C. Some laminopathies affect the cardiovascular system, and a few (namely, Dunnigan-type familial partial lipodystrophy [FPLD2] and Hutchinson-Gilford progeria syndrome [HGPS]) feature atherosclerosis as a key component. The...

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Source

Identifiers

PMID: 15205220
DOI: 10.1161/01.ATV.0000136392.59656.8b

Genes

LMNA

Provenance

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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