Extracellular Prion Protein Aggregates in Nine Gerstmann–Sträussler–Scheinker Syndrome Subjects with Mutation P102L: A Micromorphological Study and Comparison with Literature Data

Gerstmann–Sträussler–Scheinker syndrome (GSS) is a hereditary neurodegenerative disease characterized by extracellular aggregations of pathological prion protein (PrP) forming characteristic plaques. Our study aimed to evaluate the micromorphology and protein composition of these plaques in relation...

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Detalles Bibliográficos
Autores principales: Jankovska, Nikol, Matej, Radoslav, Olejar, Tomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704598/
https://www.ncbi.nlm.nih.gov/pubmed/34948096
http://dx.doi.org/10.3390/ijms222413303

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704598/
https://www.ncbi.nlm.nih.gov/pubmed/34948096
http://dx.doi.org/10.3390/ijms222413303

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