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Article

Analysis of genetic variations of lamin A/C gene (LMNA) by denaturing high-performance liquid chromatography.

Journal of biomolecular screening - 1 Oct 2004

Taylor Matthew R G, Robinson Misi L, Mestroni Luisa

Abstract excerpt

The human LMNA gene, when mutated, has been shown to cause at least 7 human diseases: dilated cardiomyopathy, Emery Dreifuss muscular dystrophy, limb girdle muscular dystrophy, familial partial lipodystrophy, Charcot Marie tooth disease type II, mandibuloacral dysplasia, and Hutchinson-Gilford Progeria (OMIM #176670). This article describes a high-throughput method for screening the human lamin A/C (LMNA) gene...

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Share to Cardiomyopathy, Dilated
Share to Chromatography, High Pressure Liquid

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 15475483
DOI: 10.1177/1087057104266393

Genes

LMNA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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Analysis of genetic variations of lamin A/C gene (LMNA) by denaturing high-performance liquid chromatography.PMID 15475483Read ↗

Mutations in the LMNA gene encoding lamin A/C.Semantic proximity Read ↗

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Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.Semantic proximity Read ↗

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