Myogenic program dysregulation is contributory to disease pathogenesis in spinal muscular atrophy

Mutations in the survival motor neuron (SMN1) gene lead to the neuromuscular disease spinal muscular atrophy (SMA). Although SMA is primarily considered as a motor neuron disease, the importance of muscle defects in its pathogenesis has not been fully examined. We use both primary cell culture and t...

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Detalles Bibliográficos
Autores principales: Boyer, Justin G., Deguise, Marc-Olivier, Murray, Lyndsay M., Yazdani, Armin, De Repentigny, Yves, Boudreau-Larivière, Céline, Kothary, Rashmi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103674/
https://www.ncbi.nlm.nih.gov/pubmed/24691550
http://dx.doi.org/10.1093/hmg/ddu142

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