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Erratum to: R208H-129VV haplotype in the prion protein gene: phenotype and neuroimaging of a patient with genetic Creutzfeldt-Jakob disease

✍ Scribed by Vita, Maria Gabriella; Gaudino, Simona; Giuda, Daniela; Sauchelli, Donato; Alboini, Paolo Emilio; Gangemi, Emma; Bizzarro, Alessandra; Scaricamazza, Eugenia; Capellari, Sabina; Parchi, Piero; Masullo, Carlo


Book ID
121597114
Publisher
Springer
Year
2013
Tongue
English
Weight
95 KB
Volume
260
Category
Article
ISSN
0340-5354

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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