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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.

Angelina CistaroL CassaliaC FerraraC AtzoriD VaiN QuartuccioP FaniaG P VaudanoD Imperiale
Published in: Journal of neurology (2016)
Keyphrases
  • genome wide
  • copy number
  • early onset
  • white matter
  • resting state
  • dna methylation
  • cerebral ischemia
  • gene expression