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Article

Lamin A/C truncation in dilated cardiomyopathy with conduction disease.

BMC medical genetics - 10 Jul 2003

MacLeod Heather M, Culley Mary R, Huber Jill M, McNally Elizabeth M

Abstract excerpt

BACKGROUND: Mutations in the gene encoding the nuclear membrane protein lamin A/C have been associated with at least 7 distinct diseases including autosomal dominant dilated cardiomyopathy with conduction system disease, autosomal dominant and recessive Emery Dreifuss Muscular Dystrophy, limb girdle muscular dystrophy type 1B, autosomal recessive type 2 Charcot Marie Tooth, mandibuloacral dysplasia, familial...

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Source

Open in PubMed Open full text

Identifiers

PMID: 12854972
DOI: 10.1186/1471-2350-4-4
PMCID: PMC169171

Genes

LMNA

Variants

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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