Codon 200 mutation in a new family of Chilean origin with Creutzfeldt-Jakob disease.

Podobné jednotky

• Codon 219 polymorphism of PRNP in healthy Caucasians and Creutzfeldt-Jakob disease patients.
  Autor: Petraroli, R., a další
  Vydáno: (1996)
• Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.
  Autor: Lee, H S, a další
  Vydáno: (1999)
• Age at Death of Creutzfeldt-Jakob disease in subsequent family generation carrying the E200K mutation of the prion protein gene.
  Autor: Maurizio Pocchiari, a další
  Vydáno: (2013-01-01)
• Age at Death of Creutzfeldt-Jakob Disease in Subsequent Family Generation Carrying the E200K Mutation of the Prion Protein Gene
  Autor: Pocchiari, Maurizio, a další
  Vydáno: (2013)
• Clinical heterogeneity and unusual presentations of Creutzfeldt-Jakob disease in Jewish patients with the PRNP codon 200 mutation.
  Autor: Chapman, J, a další
  Vydáno: (1993)