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Article

LMNA mutation in a 45 year old Japanese subject with Hutchinson-Gilford progeria syndrome.

Journal of medical genetics - 1 May 2004

Fukuchi K, Katsuya T, Sugimoto K, Kuremura M, Kim H D, Li L, Ogihara T

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Topics

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 15121795
DOI: 10.1136/jmg.2003.014688
PMCID: PMC1735754

Genes

LMNA

Provenance

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Related research

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Research trail→

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LMNA mutation in a 45 year old Japanese subject with Hutchinson-Gilford progeria syndrome.PMID 15121795Read ↗

Hutchinson-Gilford progeria syndrome: report of 2 cases and a novel LMNA mutation of HGPS in China.Semantic proximity Read ↗

Hutchinson-Gilford progeria syndrome caused by an LMNA mutation: a case report.Semantic proximity Read ↗

Unraveling the mysteries of Hutchinson-Gilford progeria syndrome: a comprehensive review of LMNA gene mutations.Semantic proximity Read ↗

Homozygous LMNA mutation R527C in atypical Hutchinson-Gilford progeria syndrome: evidence for autosomal recessive inheritance.Semantic proximity Read ↗

[Three cases of Hutchinson-Gilford progeria syndrome].Semantic proximity Read ↗

p.Pro4Arg mutation in LMNA gene: a new atypical progeria phenotype without metabolism abnormalities.Semantic proximity Read ↗

Hutchinson-Gilford progeria syndrome.Semantic proximity Read ↗

Hutchinson-Gilford Progeria Syndrome: A Premature Aging Disease.Semantic proximity Read ↗

An inherited LMNA gene mutation in atypical Progeria syndrome.Semantic proximity Read ↗

LMNA mutation in progeroid syndrome in association with strokes.Semantic proximity Read ↗

LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090).Semantic proximity Read ↗

Novel LMNA gene mutation in a patient with Atypical Werner's Syndrome.Semantic proximity Read ↗

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