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Experimental Models of Inherited PrP Prion Diseases
The inherited prion protein (PrP) prion disorders, which include familial Creutzfeldt–Jakob disease, Gerstmann–Sträussler–Scheinker disease, and fatal familial insomnia, constitute ∼10%–15% of all PrP prion disease cases in humans. Attempts to generate animal models of these disorders using transgen...
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| Publicado en: | Cold Spring Harb Perspect Med |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Cold Spring Harbor Laboratory Press
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5513788/ https://ncbi.nlm.nih.gov/pubmed/28096244 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1101/cshperspect.a027151 |
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