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3. Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease. Worrall BB; Herman ST; Capellari S; Lynch T; Chin S; Gambetti P; Parchi P J Neurol Neurosurg Psychiatry; 1999 Nov; 67(5):671-4. PubMed ID: 10519879 [TBL] [Abstract][Full Text] [Related]
4. 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]
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