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

Ítems similars

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