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Article

Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy.

Muscle & nerve - 1 Nov 1993

Yoshida K, Ikeda S, Nakamura A, Kagoshima M, Takeda S, Shoji S, Yanagisawa N

Abstract excerpt

Molecular analysis of the Duchenne muscular dystrophy (DMD) gene was performed on 4 unrelated patients with Becker muscular dystrophy (BMD) presenting with dilated cardiomyopathy. Two patients with a deletion involving exon 1 were quite unique in that they developed fatal myocardial involvement in their teens, despite the absence of significant muscular weakness. The deletion found in these patients comprised the...

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Identifiers

PMID: 8413368
DOI: 10.1002/mus.880161104

Genes

DMD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular analysis of the Duchenne muscular dystrophy gene in patients with Becker muscular dystrophy presenting with dilated cardiomyopathy.PMID 8413368Read ↗

Phenotypic Characterization of a Family With An In-frame Deletion in the DMD Gene and Variable Penetrance.Semantic proximity Read ↗

Analysis of Dystrophin Deletion Mutations Predicts Age of Cardiomyopathy Onset in Becker Muscular DystrophySemantic proximity Read ↗

A novel dystrophin deletion mutation in a becker muscular dystrophy patient with early-onset dilated cardiomyopathy.Semantic proximity Read ↗

Large in-frame deletions of the rod-shaped domain of the dystrophin gene resulting in severe phenotype.Semantic proximity Read ↗

Follow-up of three patients with a large in-frame deletion of exons 45-55 in the Duchenne muscular dystrophy (DMD) gene.Semantic proximity Read ↗

Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.Semantic proximity Read ↗

[Molecular genetics of Duchenne/Becker muscular dystrophy].Semantic proximity Read ↗

Molecular characterization of exonic rearrangements and frame shifts in the dystrophin gene in Duchenne muscular dystrophy patients in a Saudi community.Semantic proximity Read ↗

DNA sequence analysis for structure/function and mutation studies in Becker muscular dystrophy.Semantic proximity Read ↗

Further evidence for an attenuated phenotype of in-frame DMD deletions affecting the central rod domain of dystrophin around exon 48.Semantic proximity Read ↗

Clinical characterisation of Becker muscular dystrophy patients predicts favourable outcome in exon-skipping therapySemantic proximity Read ↗

Mutation spectrum leading to an attenuated phenotype in dystrophinopathies.Semantic proximity Read ↗

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