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A novel form of human disease with a protease-sensitive prion protein and heterozygosity methionine/valine at codon 129: Case report

Rodríguez Martínez, Ana B.; Garrido, Joseba M.; Zarranz Imirizaldu, Juan José; Arteagoitia, Jose M.;; Martínez de Pancorbo Gómez, María de los Angeles; Atares, Begona;; Bilbao, Miren J.;; Ferrer, Isidro;; Juste, Ramon A.; (BioMed Central, 2010-10)

Background: Sporadic Creutzfeldt-Jakob disease (sCJD) is a rare neurodegenerative disorder in humans included in the group of Transmissible Spongiform Encephalopathies or prion diseases. The vast majority of sCJD cases are ...