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Article

Duchenne muscular dystrophy: a clinical, histopathological and genetic study at a neurology tertiary care center in Southern India.

Neurology India - 1 Jan 2000

Swaminathan Bhairavi, Shubha G N, Shubha D, Murthy A Ram, Kiran Kumar H B, Shylashree S, Gayathri N, Jamuna R, Jain Sanjeev, Purushottam Meera, Nalini A

Abstract excerpt

BACKGROUND: Duchenne muscular dystrophy (DMD) is the most common muscular dystrophy that affects young boys and the dystrophin gene on the X chromosome has been found to be associated with the disorder. MATERIALS AND METHODS: In this prospective study, 112 clinically diagnosed DMD patients had mu...

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Identifiers

PMID: 20139501
DOI: 10.4103/0028-3886.59468

Genes

DMD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20139501-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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