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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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Detalles Bibliográficos
Autores principales:	Jeong, Byung-Hoon, Kim, Yong-Sun
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	The Korean Academy of Medical Sciences 2014
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4024956/ https://www.ncbi.nlm.nih.gov/pubmed/24851016 http://dx.doi.org/10.3346/jkms.2014.29.5.623

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