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Genetic Creutzfeldt‐Jakob disease (gCJD) with a methionine to arginine substitution at codon 232 of the prion protein gene (gCJD‐M232R) is rare and has only been reported in Japan. We report an autopsy case of gCJD‐M232R showing alleles of codon 129 that were homozygous for methionine and the presence of multiple strains of the protease‐resistant, abnormal isoform of prion protein (PrPSc), M1 + M2C...
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