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16. Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene. Komatsu J; Sakai K; Hamaguchi T; Sugiyama Y; Iwasa K; Yamada M Prion; 2014; 8(5):336-8. PubMed ID: 25495585 [TBL] [Abstract][Full Text] [Related]
17. Novel PRNP mutation in a patient with a slow progressive dementia syndrome. Heinemann U; Krasnianski A; Meissner B; Grasbon-Frodl EM; Kretzschmar HA; Zerr I Med Sci Monit; 2008 May; 14(5):CS41-43. PubMed ID: 18443555 [TBL] [Abstract][Full Text] [Related]
18. Creutzfeldt-Jakob disease: report of four cases and review of the literature. Atalay FÖ; Tolunay Ş; Özgün G; Bekar A; Zarifoğlu M Turk Patoloji Derg; 2015; 31(2):148-52. PubMed ID: 24272930 [TBL] [Abstract][Full Text] [Related]
19. [A case of codon 232 mutation-induced Creutzfeldt-Jakob disease visualized by the MRI-FLAIR images with atypical clinical symptoms]. Saito T; Isozumi K; Komatsumoto S; Nara M; Suzuki K; Dohura K Rinsho Shinkeigaku; 2000 Jan; 40(1):51-4. PubMed ID: 10825802 [TBL] [Abstract][Full Text] [Related]
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