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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...
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| Publicado no: | Biomolecules |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
MDPI
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7912988/ https://ncbi.nlm.nih.gov/pubmed/33540845 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/biom11020207 |
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