Clinical and Genetic Study of Algerian Patients with Spinal Muscular Atrophy

Spinal muscular atrophy (SMA) is the second most common lethal autosomal recessive disorder. It is divided into the acute Werdnig-Hoffmann disease (type I), the intermediate form (type II), the Kugelberg-Welander disease (type III), and the adult form (type IV). The gene involved in all four forms o...

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Detalles Bibliográficos
Autores principales: Sifi, Y., Sifi, K., Boulefkhad, A., Abadi, N., Bouderda, Z., Cheriet, R., Magen, M., Bonnefont, J. P., Munnich, A., Benlatreche, C., Hamri, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Clinical Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437343/
https://www.ncbi.nlm.nih.gov/pubmed/26317002
http://dx.doi.org/10.1155/2013/903875

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4437343/
https://www.ncbi.nlm.nih.gov/pubmed/26317002
http://dx.doi.org/10.1155/2013/903875

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