An atypical phenotype of Creutzfeldt-Jakob Disease(CJD) associated with the E200K mutation in the prion protein gene.

Carlo Masullo, Sabina Capellari, Piero Parchi

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)
Original languageEnglish
Pages (from-to)837-839
Number of pages3
JournalNeurological Sciences
Volume31
Publication statusPublished - 2010

Keywords

  • Creutzfeldt-Jakob Disease
  • Diagnosis
  • E200K genotype
  • PRNP gene
  • Phenotype
  • Point Mutations
  • Prion Diseases

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