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Alpha-Synuclein Loss in Spinal Muscular Atrophy
Spinal muscular atrophy, the most prevalent hereditary motor neuron disease, is caused by mutations in the survival motor neuron (SMN) 1 gene. A significant reduction in the encoded SMN protein leads to the degeneration of motor neurons. However, the molecular events leading to this process are not...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3918138/ https://ncbi.nlm.nih.gov/pubmed/20640532 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12031-010-9422-1 |
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