Familial Creutzfeldt–Jakob Disease with a PRNP Mutation at Codon 180 Presented with Visual Hallucinations and Illusions

Podobne zapisy

• Familial Creutzfeldt-Jakob Disease with V180I Mutation
  od: Yang, Tae-Il, i wsp.
  Wydane: (2010)
• Codon 219 polymorphism of PRNP in healthy Caucasians and Creutzfeldt-Jakob disease patients.
  od: Petraroli, R., i wsp.
  Wydane: (1996)
• Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes
  od: Diack, Abigail B, i wsp.
  Wydane: (2019)
• Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes
  Wydane: (2019)
• Rare V180I mutation in PRNP gene of a Chinese patient with Creutzfeldt-Jakob disease
  od: Shi, Qi, i wsp.
  Wydane: (2014)