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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

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