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Article

Duchenne and Becker muscular dystrophy: contribution of a molecular and immunohistochemical analysis in diagnosis in Morocco.

Journal of biomedicine & biotechnology - 1 Jan 2009

Bellayou Hanane, Hamzi Khalil, Rafai Mohamed Abdou, Karkouri Mehdi, Slassi Ilham, Azeddoug Houssine, Nadifi Sellama

Abstract excerpt

Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked recessive disorders caused by mutations of the DMD gene located at Xp21. In DMD patients, dystrophin is virtually absent; whereas BMD patients have 10% to 40% of the normal amount. Deletions in the dystrophin gene represent 65% of mutations in DMD/BMD patients. To explain the contribution of immunohistochemical and genetic analysis...

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Source

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Identifiers

PMID: 19461958
DOI: 10.1155/2009/325210
PMCID: PMC2683945

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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