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Article

Screening of dystrophin gene deletions in Egyptian patients with DMD/BMD muscular dystrophies.

Disease markers - 1 Jan 2000

Effat L K, El-Harouni A A, Amr K S, El-Minisi T I, Abdel Meguid N, El-Awady M

Abstract excerpt

Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are allelic disorders caused by mutations within the dystrophin gene. Our study has identified 100 Egyptian families collected from the Human Genetics Clinic, National Research Center, Cairo. All cases were subjected to complete clinical evaluation pedigree analysis, electromyography studies, estimation of serum creatine phosphokinase enzyme...

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Source

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Identifiers

PMID: 11381192
DOI: 10.1155/2000/437372
PMCID: PMC3851408

Genes

DMD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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