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Article

Evolving molecular diagnostics for familial cardiomyopathies: at the heart of it all.

Expert review of molecular diagnostics - 1 Apr 2010

Callis Thomas E, Jensen Brian C, Weck Karen E, Willis Monte S

Abstract excerpt

Cardiomyopathies are an important and heterogeneous group of common cardiac diseases. An increasing number of cardiomyopathies are now recognized to have familial forms, which result from single-gene mutations that render a Mendelian inheritance pattern, including hypertrophic cardiomyopathy, dilated cardiomyopathy, restrictive cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy and left ventricular...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 20370590
DOI: 10.1586/erm.10.13
PMCID: PMC5022563

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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