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Ultrastructural characterization of peripheral denervation in a mouse model of Type III spinal muscular atrophy
Spinal muscular atrophy (SMA) is a heritable, autosomal recessive neuromuscular disorder characterized by a loss of the survival of motor neurons (SMN) protein, which leads to degeneration of lower motor neurons, and muscle atrophy. Despite SMA being nosographically classified as a motor neuron dise...
Autores principales: | Fulceri, Federica, Biagioni, Francesca, Limanaqi, Fiona, Busceti, Carla L., Ryskalin, Larisa, Lenzi, Paola, Fornai, Francesco |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8205903/ https://www.ncbi.nlm.nih.gov/pubmed/33999256 http://dx.doi.org/10.1007/s00702-021-02353-9 |
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