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Prion deposition in olfactory biopsy of sporadic Creutzfeldt–Jakob disease

✍ Scribed by Massimo Tabaton; Salvatore Monaco; Maria Paola Cordone; Monica Colucci; Giorgio Giaccone; Fabrizio Tagliavini; Gianluigi Zanusso

Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
94 KB
Volume
55
Category
Article
ISSN
0364-5134

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Codon 219 lys allele of PRNP is not foun
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The polymorphism at codon 219 of the prion protein gene (PRNP) was found in the general Japanese population with 6% allele frequency. Herein, we examined 85 cases of sporadic Creutzfeldt-Jakob disease (CJD) for the codon 219 polymorphism. The codon 219G'"'Ly" heterozygous polymorphism was not found

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Inherited prion diseases are characterized by mutations in the PRNP gene encoding the prion protein (PrP). As the other sporadic or infectious prion disease forms, they are almost all characterized by the accumulation in the brain of an abnormal misfolded form of the patient's PrP. Brain extracts ca