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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Détails bibliographiques
Publié dans:J Neurodegener Dis
Auteurs principaux: Sifi, Y., Sifi, K., Boulefkhad, A., Abadi, N., Bouderda, Z., Cheriet, R., Magen, M., Bonnefont, J. P., Munnich, A., Benlatreche, C., Hamri, A.
Format: Artigo
Langue:Inglês
Publié: Hindawi Publishing Corporation 2013
Sujets:
Clinical Study
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4437343/
https://ncbi.nlm.nih.gov/pubmed/26317002
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2013/903875
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