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Article

Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.

Clinical and translational science - 1 May 2008

Hershberger Ray E, Parks Sharie B, Kushner Jessica D, Li Duanxiang, Ludwigsen Susan, Jakobs Petra, Nauman Deirdre, Burgess Donna, Partain Julie, Litt Michael

Abstract excerpt

BACKGROUND: More than 20 genes have been reported to cause idiopathic and familial dilated cardiomyopathy (IDC/FDC), but the frequency of genetic causation remains poorly understood. METHODS AND RESULTS: Blood samples were collected and DNA prepared from 313 patients, 183 with FDC and 130 with IDC. Genomic DNA underwent bidirectional sequencing of six genes, and mutation carriers were followed up by evaluation of...

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Source

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Identifiers

PMID: 19412328
DOI: 10.1111/j.1752-8062.2008.00017.x
PMCID: PMC2633921

Genes

CSRP3
MYH7
TCAP
TNNT2
LDB3

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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