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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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Detalles Bibliográficos
Autores principales: Effat, Laila K., El-Harouni, Ashraf A., Amr, Khalda S., El-Minisi, Tarik I., Abdel Meguid, Nagwa, El-Awady, Mostafa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851408/
https://www.ncbi.nlm.nih.gov/pubmed/11381192
http://dx.doi.org/10.1155/2000/437372