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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Detalhes bibliográficos
Main Authors: Effat, Laila K., El-Harouni, Ashraf A., Amr, Khalda S., El-Minisi, Tarik I., Abdel Meguid, Nagwa, El-Awady, Mostafa
Formato: Artigo
Idioma:Inglês
Publicado em: IOS Press 2000
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Acesso em linha: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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