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Brain 18F-FDG PET/CT findings in a case of genetic Creutzfeldt–Jakob disease due to V203I heterozygous mutation in the PRNP gene

Crossref DOI link: https://doi.org/10.1007/s00415-016-8327-5

Published Online: 2016-11-14

Published Print: 2017-01

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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