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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | J Neural Transm (Vienna) |
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| Κύριοι συγγραφείς: | , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Springer Vienna
2021
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8205903/ https://ncbi.nlm.nih.gov/pubmed/33999256 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00702-021-02353-9 |
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