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Article

Genotype-phenotype correlation in Duchenne/Becker muscular dystrophy patients seen at Lucknow.

The Indian journal of medical research - 1 Jan 1997

Mittal B, Singh V, Mishra S, Sinha S, Mittal R D, Chaturvedi L S, Danda S, Pradhan S, Agarwal S S

Abstract excerpt

The molecular basis of two allelic forms of muscular dystrophy, Duchenne (DMD) and Becker (BMD), has been explained by frame shift hypothesis. In order to test this hypothesis, deletional mutations in 59 patients confirmed to have DMD and 11 BMD patients were analysed using multiplex polymerase chain reaction and Southern hybridization with dystrophin cDNA probes. Translational reading frame of the dystrophin...

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Source

Identifiers

PMID: 9029833

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.

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Genotype-phenotype correlation in Duchenne/Becker muscular dystrophy patients seen at Lucknow.PMID 9029833Read ↗

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Re-evaluation of reading frame-shift hypothesis in Duchenne and Becker muscular dystrophy.Semantic proximity Read ↗

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Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large CohortSemantic proximity Read ↗

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Entries in the Leiden Duchenne muscular dystrophy mutation database: an overview of mutation types and paradoxical cases that confirm the reading-frame rule.Semantic proximity Read ↗

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