Genetic aspects of human prion diseases

Human prion diseases are rapidly progressive and fatal neurodegenerative conditions caused by a disease-causing isoform of the native prion protein. The prion protein gene (PRNP) encodes for the cellular prion protein, which is the biological substrate for prion disease transmission and neurotoxicit...

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Detalles Bibliográficos
Autores principales: Appleby, Brian S., Shetty, Shashirekha, Elkasaby, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9579322/
https://www.ncbi.nlm.nih.gov/pubmed/36277922
http://dx.doi.org/10.3389/fneur.2022.1003056

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9579322/
https://www.ncbi.nlm.nih.gov/pubmed/36277922
http://dx.doi.org/10.3389/fneur.2022.1003056

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