๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Distribution of prion protein in German patients with Creutzfeldt-Jakob disease is different from that in Japanese patients

โœ Scribed by R. Doi-Yi; T. Kitamoto; K. Ogomori; P. Mehraein; J. Tateishi


Publisher
Springer-Verlag
Year
1994
Tongue
English
Weight
639 KB
Volume
87
Category
Article
ISSN
0001-6322

No coin nor oath required. For personal study only.


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