Screening of Dystrophin Gene Deletions in Egyptian Patients with DMD/BMD Muscular Dystrophies

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 c...

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Bibliografiske detaljer
Main Authors: Effat, Laila K., El-Harouni, Ashraf A., Amr, Khalda S., El-Minisi, Tarik I., Abdel Meguid, Nagwa, El-Awady, Mostafa
Format: Artigo
Sprog:Inglês
Udgivet: IOS Press 2000
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Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3851408/
https://ncbi.nlm.nih.gov/pubmed/11381192
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2000/437372
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