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Article

Lamin A/C mutations associated with familial and sporadic cases of dilated cardiomyopathy in Koreans.

Experimental & molecular medicine - 28 Feb 2007

Song Kyuyoung, Dubé Marie Pierre, Lim Jiyoung, Hwang Ilsun, Lee Inchul, Kim Jae-Joong

Abstract excerpt

Dilated cardiomyopathy (DCM) is characterized by cardiac dilation and systolic dysfunction. So far sixteen genes have been shown to cause autosomal dominant familial dilated cardiomyopathy (FDC). We identified a large Korean family from the Jeju island showing a clear Mendelian inheritance of FDC. A genomewide linkage scan at 9 cM marker density identified a peak multipoint LOD score of 2.82 at D1S195....

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Source

Identifiers

PMID: 17334235
DOI: 10.1038/emm.2007.13

Genes

LMNA

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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