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Mutant Prion Protein D202N Associated with Familial Prion Disease is Retained in the Endoplasmic Reticulum and Forms ‘Curly’ Intracellular Aggregates
Transmissible Spongiform Encephalopathies are fatal neurodegenerative disorders of humans and animals that are familial, sporadic, and infectious in nature. Familial disorders of humans include Gerstmann–Straussler–Scheinker disease (GSS), familial Creutzfeldt–Jakob disease (CJD), and fatal familial...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2394189/ https://ncbi.nlm.nih.gov/pubmed/17873292 |
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