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Amyotrophic Lateral Sclerosis: Proteins, Proteostasis, Prions, and Promises
Amyotrophic lateral sclerosis (ALS) is characterized by the progressive degeneration of the motor neurons that innervate muscle, resulting in gradual paralysis and culminating in the inability to breathe or swallow. This neuronal degeneration occurs in a spatiotemporal manner from a point of onset i...
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| Publicado no: | Front Cell Neurosci |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Frontiers Media S.A.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7671971/ https://ncbi.nlm.nih.gov/pubmed/33328890 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2020.581907 |
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