Co-existence of PrP(D) types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics

We report a detailed study of a cohort of sporadic Creutzfeldt-Jakob disease (sCJD) VV1–2 type-mixed cases (valine homozygosity at codon 129 of the prion protein, PrP, gene harboring disease-related PrP, PrP(D), types 1 and 2). Overall, sCJDVV1–2 subjects showed mixed clinical and histopathological...

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Detalles Bibliográficos
Autores principales: Cali, Ignazio, Puoti, Gianfranco, Smucny, Jason, Curtiss, Paul Michael, Cracco, Laura, Kitamoto, Tetsuyuki, Occhipinti, Rossana, Cohen, Mark Lloyd, Appleby, Brian Stephen, Gambetti, Pierluigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992672/
https://www.ncbi.nlm.nih.gov/pubmed/32001774
http://dx.doi.org/10.1038/s41598-020-58446-0

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6992672/
https://www.ncbi.nlm.nih.gov/pubmed/32001774
http://dx.doi.org/10.1038/s41598-020-58446-0

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