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Article

The genetics of dilated cardiomyopathy: a prioritized candidate gene study of LMNA, TNNT2, TCAP, and PLN.

Clinical cardiology - 1 Oct 2013

Hirtle-Lewis Marika, Desbiens Katia, Ruel Isabelle, Rudzicz Nicholas, Genest Jacques, Engert James C, Giannetti Nadia

Abstract excerpt

BACKGROUND: Dilated cardiomyopathy (DCM), which is characterized by left ventricular enlargement and systolic dysfunction, is divided into cases with a clear predisposing condition (eg, hypothyroidism, chemotherapeutic agents, alcoholism, ischemia) and those of unknown cause (idiopathic DCM). Many cases (20%-35%) of DCM are familial, implicating a genetic contribution to the etiology. More than 30 genes have been...

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Source

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Identifiers

PMID: 24037902
DOI: 10.1002/clc.22193
PMCID: PMC6649360

Genes

LMNA
PLN
TNNT2
TCAP

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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