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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Autori principali: Effat, Laila K., El-Harouni, Ashraf A., Amr, Khalda S., El-Minisi, Tarik I., Abdel Meguid, Nagwa, El-Awady, Mostafa
Natura: Artigo
Lingua:Inglês
Pubblicazione: IOS Press 2000
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Accesso online: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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