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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Bibliographic Details
Published in:J Neurodegener Dis
Main Authors: 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
Language:Inglês
Published: Hindawi Publishing Corporation 2013
Subjects:
Clinical Study
Online Access: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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