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Article

Becker muscular dystrophy in Indian patients: analysis of dystrophin gene deletion patterns.

Neurology India - 1 Jan 2000

Dastur Rashna S, Gaitonde Pradnya S, Khadilkar Satish V, Nadkarni Jayshree J

Abstract excerpt

BACKGROUND: Becker muscular dystrophy (BMD) is caused by mutations in the dystrophin gene with variable phenotypes. Becker muscular dystrophy patients have low levels of nearly full-length dystrophin and carry in-frame mutations, which allow partial functioning of the protein. AIM: To study the deletion patterns of BMD and to correlate the same with reading frame rule and different phenotypes. SETTING: A tertiary...

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Identifiers

PMID: 18974567
DOI: 10.4103/0028-3886.40961

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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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