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The neuroprotective factor Wld(s) fails to mitigate distal axonal and neuromuscular junction (NMJ) defects in mouse models of spinal muscular atrophy

Spinal muscular atrophy (SMA) is a common autosomal recessive neurodegenerative disorder in humans. Amongst the earliest signs of neurodegeneration are severe and progressive defects of the neuromuscular synapse. These defects, characterized by poor terminal arborization and immature motor endplates...

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Main Authors: Kariya, Shingo, Mauricio, Rina, Dai, Ya, Monani, Umrao R.
格式: Artigo
語言:Inglês
出版: 2008
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC2671206/
https://ncbi.nlm.nih.gov/pubmed/19010394
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neulet.2008.10.107
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