Incidence and spectrum of sporadic Creutzfeldt–Jakob disease variants with mixed phenotype and co-occurrence of PrP(Sc) types: an updated classification

Six subtypes of sporadic Creutzfeldt–Jakob disease with distinctive clinico-pathological features have been identified largely based on two types of the abnormal prion protein, PrP(Sc), and the methionine (M)/valine (V) polymorphic codon 129 of the prion protein. The existence of affected subjects s...

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Detalles Bibliográficos
Autores principales: Parchi, Piero, Strammiello, Rosaria, Notari, Silvio, Giese, Armin, Langeveld, Jan P. M., Ladogana, Anna, Zerr, Inga, Roncaroli, Federico, Cras, Patrich, Ghetti, Bernardino, Pocchiari, Maurizio, Kretzschmar, Hans, Capellari, Sabina
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2773124/
https://www.ncbi.nlm.nih.gov/pubmed/19718500
http://dx.doi.org/10.1007/s00401-009-0585-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2773124/
https://www.ncbi.nlm.nih.gov/pubmed/19718500
http://dx.doi.org/10.1007/s00401-009-0585-1

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