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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Autores principales: Effat, Laila K., El-Harouni, Ashraf A., Amr, Khalda S., El-Minisi, Tarik I., Abdel Meguid, Nagwa, El-Awady, Mostafa
Formato: Artigo
Lenguaje:Inglês
Publicado: IOS Press 2000
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Acceso en línea: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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