Molecular Mechanisms of Neurodegeneration in Spinal Muscular Atrophy

Spinal muscular atrophy (SMA) is an autosomal recessive motor neuron disease with a high incidence and is the most common genetic cause of infant mortality. SMA is primarily characterized by degeneration of the spinal motor neurons that leads to skeletal muscle atrophy followed by symmetric limb par...

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Detalles Bibliográficos
Autores principales: Ahmad, Saif, Bhatia, Kanchan, Kannan, Annapoorna, Gangwani, Laxman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2016
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807884/
https://www.ncbi.nlm.nih.gov/pubmed/27042141
http://dx.doi.org/10.4137/JEN.S33122

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807884/
https://www.ncbi.nlm.nih.gov/pubmed/27042141
http://dx.doi.org/10.4137/JEN.S33122

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