Molecular Pathology of Human Prion Diseases

Prion diseases are fatal neurodegenerative conditions in humans and animals. In this review, we summarize the molecular background of phenotypic variability, relation of prion protein (PrP) to other proteins associated with neurodegenerative diseases, and pathogenesis of neuronal vulnerability. PrP...

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Detalles Bibliográficos
Autores principales: Kovacs, Gabor G., Budka, Herbert
Formato: Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2009
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2672014/
https://www.ncbi.nlm.nih.gov/pubmed/19399233
http://dx.doi.org/10.3390/ijms10030976

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2672014/
https://www.ncbi.nlm.nih.gov/pubmed/19399233
http://dx.doi.org/10.3390/ijms10030976

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