Gerstmann–Sträussler–Scheinker Disease with F198S Mutation Induces Independent Tau and Prion Protein Pathologies in Bank Voles

Gerstmann–Sträussler–Scheinker disease (GSS) is a rare genetic prion disease. A large GSS kindred linked to the serine-for-phenylalanine substitution at codon 198 of the prion protein gene (GSS-F198S) is characterized by conspicuous accumulation of prion protein (PrP)-amyloid deposits and neurofibri...

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Detalles Bibliográficos
Autores principales: Bruno, Rosalia, Pirisinu, Laura, Riccardi, Geraldina, D’Agostino, Claudia, De Cecco, Elena, Legname, Giuseppe, Cardone, Franco, Gambetti, Pierluigi, Nonno, Romolo, Agrimi, Umberto, Di Bari, Michele Angelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599806/
https://www.ncbi.nlm.nih.gov/pubmed/36291746
http://dx.doi.org/10.3390/biom12101537

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599806/
https://www.ncbi.nlm.nih.gov/pubmed/36291746
http://dx.doi.org/10.3390/biom12101537

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