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Article

[Hutchinson-Gilford progeria in the light of contemporary genetics].

Medycyna wieku rozwojowego - 1 Jan 2000

Madej-Pilarczyk Agnieszka

Abstract excerpt

Hutchinson-Gilford progeria causing premature aging of children is a genetic disease and according to most authors has an autosomal dominant inheritance. It has been regarded as a model of the process of aging. In 2003 mutations in the LMNA gene, localized f in chromosome 1, responsible for the disease, were identified. The most frequent mutation is located in exon 11, C1824T and does not change glycin in...

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Source

Identifiers

PMID: 17028399

Genes

LMNA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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