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...

Descripción completa

Detalles Bibliográficos
Autores principales: Bellayou, Hanane, Hamzi, Khalil, Rafai, Mohamed Abdou, Karkouri, Mehdi, Slassi, Ilham, Azeddoug, Houssine, Nadifi, Sellama
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2009
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683945/
https://www.ncbi.nlm.nih.gov/pubmed/19461958
http://dx.doi.org/10.1155/2009/325210

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2683945/
https://www.ncbi.nlm.nih.gov/pubmed/19461958
http://dx.doi.org/10.1155/2009/325210

Ejemplares similares