Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene.

Podobne zapisy

• Creutzfeldt–Jakob disease in a Chinese patient with a novel seven extra‐repeat insertion in PRNP
  od: Wang, X F, i wsp.
  Wydane: (2007)
• Creutzfeldt–Jakob disease in a Chinese patient with a novel seven extra-repeat insertion in PRNP
  od: Wang, X F, i wsp.
  Wydane: (2009)
• Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.
  od: Chapman, J, i wsp.
  Wydane: (1993)
• Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.
  od: Lee, H S, i wsp.
  Wydane: (1999)
• Phenotype-genotype studies in kuru: Implications for new variant Creutzfeldt–Jakob disease
  od: Cervenáková, Larisa, i wsp.
  Wydane: (1998)