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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Библиографические подробности
Главные авторы: Boyer, Justin G., Deguise, Marc-Olivier, Murray, Lyndsay M., Yazdani, Armin, De Repentigny, Yves, Boudreau-Larivière, Céline, Kothary, Rashmi
Формат: Artigo
Язык:Inglês
Опубликовано: Oxford University Press 2014
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Articles
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4103674/
https://ncbi.nlm.nih.gov/pubmed/24691550
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu142
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