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Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt–Jakob Disease phenotype

✍ Scribed by Bart Van Everbroeck; Esther A. Croes; Philippe Pals; Bart Dermaut; Gerard Jansen; Cornelia M. van Duijn; Marc Cruts; Christine Van Broeckhoven; Jean-Jacques Martin; Patrick Cras

Book ID: 117472159
Publisher: Elsevier Science
Year: 2001
Tongue: English
Weight: 80 KB
Volume: 313
Category: Article
ISSN: 0304-3940
DOI: 10.1016/s0304-3940(01)02264-9

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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