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Fragmentation of the Golgi apparatus of the ballooned neurons in patients with corticobasal degeneration and Creutzfeldt-Jakob disease

✍ Scribed by A. Sakurai; K. Okamoto; Y. Fujita; Y. Nakazato; K. Wakabayashi; H. Takahashi; N. K. Gonatas


Publisher
Springer-Verlag
Year
2000
Tongue
English
Weight
205 KB
Volume
100
Category
Article
ISSN
0001-6322

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Polymorphisms of the prion protein gene
✍ Mirella Salvatore; Maurizio Genuardi; Rosella Petraroli; Carlo Masullo; Marco D' πŸ“‚ Article πŸ“… 1994 πŸ› Springer 🌐 English βš– 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