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Genetic Studies in Human Prion Diseases
Human prion diseases are fatal neurodegenerative disorders that are characterized by spongiform changes, astrogliosis, and the accumulation of an abnormal prion protein (PrP(Sc)). Approximately 10%-15% of human prion diseases are familial variants that are caused by pathogenic mutations in the prion...
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| Huvudupphovsmän: | , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
The Korean Academy of Medical Sciences
2014
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| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4024956/ https://ncbi.nlm.nih.gov/pubmed/24851016 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3346/jkms.2014.29.5.623 |
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