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Article

Lamin A/C gene mutation associated with dilated cardiomyopathy with variable skeletal muscle involvement.

Circulation - 8 Feb 2000

Brodsky G L, Muntoni F, Miocic S, Sinagra G, Sewry C, Mestroni L

Abstract excerpt

BACKGROUND: Dilated cardiomyopathy is a form of heart muscle disease characterized by impaired systolic function and ventricular dilation. Familial transmission of the disease is frequently observed, and genetic heterogeneity is indicated by clinical and morphological variability in the disease phenotype. In the family MDDC1 reported here, the disease phenotype is severe and characterized by an autosomal dominant...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 10662742
DOI: 10.1161/01.cir.101.5.473

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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