Duchenne and Becker Muscular Dystrophy: Contribution of a Molecular and Immunohistochemical Analysis in Diagnosis in Morocco

Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are X-linked recessive disorders caused by mutations of the DMD gene located at Xp21. In DMD patients, dystrophin is virtually absent; whereas BMD patients have 10% to 40% of the normal amount. Deletions in the dystrophin gene rep...

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Detalhes bibliográficos
Main Authors: Bellayou, Hanane, Hamzi, Khalil, Rafai, Mohamed Abdou, Karkouri, Mehdi, Slassi, Ilham, Azeddoug, Houssine, Nadifi, Sellama
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi Publishing Corporation 2009
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2683945/
https://ncbi.nlm.nih.gov/pubmed/19461958
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2009/325210
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