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Article

R25G mutation in exon 1 of LMNA gene is associated with dilated cardiomyopathy and limb-girdle muscular dystrophy 1B.

Chinese medical journal - 5 Dec 2009

Yuan Wo-liang, Huang Chun-yan, Wang Jing-feng, Xie Shuang-lun, Nie Ru-qiong, Liu Ying-mei, Liu Pin-ming, Zhou Shu-xian, Chen Su-qin, Huang Wei-jun

Abstract excerpt

BACKGROUND: Mutations of the LMNA gene encoding lamin A and C are associated with dilated cardiomyopathy (DCM), conduction system defects and skeletal muscle dystrophy. Here we report a family with a mutation of the LMNA gene to identify the relationship between genotype and phenotype. METHODS: A...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20092787

Genes

LMNA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-20092787-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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R25G mutation in exon 1 of LMNA gene is associated with dilated cardiomyopathy and limb-girdle muscular dystrophy 1B.PMID 20092787Read ↗

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Expanding the phenotype of LMNA mutations in dilated cardiomyopathy and functional consequences of these mutations.Semantic proximity Read ↗

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