Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients

Duchenne and Becker muscular dystrophy (DMD and BMD) are X-linked diseases resulting from a defect in the dystrophin gene located on Xp21. DMD is the most frequent neuromuscular disease in humans (1/3500 male newborn). Deletions in the dystrophin gene represent 65% of mutations in DMD/BMD patients....

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Detalles Bibliográficos
Autores principales: Sbiti, Aziza, El Kerch, Fatiha, Sefiani, Abdelaziz
Formato: Texto
Lenguaje:English
Publicado: 2002
Materias:
Correspondence Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC161366/
https://www.ncbi.nlm.nih.gov/pubmed/12488581
http://dx.doi.org/10.1155/S1110724302205069

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC161366/
https://www.ncbi.nlm.nih.gov/pubmed/12488581
http://dx.doi.org/10.1155/S1110724302205069

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