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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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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2002
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC161366/ https://ncbi.nlm.nih.gov/pubmed/12488581 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/S1110724302205069 |
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