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Deposition of the prion protein (PrP) during the evolution of experimental Creutzfeldt-Jakob disease

โœ Scribed by Radzislaw Kordek; Johannes A. Hainfellner; Pawel P. Liberski; H. Budka


Publisher
Springer-Verlag
Year
1999
Tongue
English
Weight
421 KB
Volume
98
Category
Article
ISSN
0001-6322

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๐Ÿ“œ SIMILAR VOLUMES


Polymorphisms of the prion protein gene
โœ Mirella Salvatore; Maurizio Genuardi; Rosella Petraroli; Carlo Masullo; Marco D' ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Springer ๐ŸŒ English โš– 593 KB

Creutzfeldt-Jakob disease (CJD) is a transmissible neurodegenerative disorder characterized by the accumulation of the amyloid protein PrP in the CNS. Two coding polymorphisms of the PrP gene (PRNP) are a methionine (Met) to valine (Val) change at codon 129, and a deletion in the octapeptide coding