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Prion Diseases: A Unique Transmissible Agent or a Model for Neurodegenerative Diseases?
The accumulation and propagation in the brain of misfolded proteins is a pathological hallmark shared by many neurodegenerative diseases such as Alzheimer’s disease (Aβ and tau), Parkinson’s disease (α-synuclein), and prion disease (prion protein). Currently, there is no epidemiological evidence to...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2021
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7912988/ https://www.ncbi.nlm.nih.gov/pubmed/33540845 http://dx.doi.org/10.3390/biom11020207 |