Mutations at codons 178, 200-129, and 232 contributed to the inherited prion diseases in Korean patients

פריטים דומים

• Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphism.
  מאת: Medori, R, et al.
  יצא לאור: (1993)
• Codon 129 changes in the prion protein gene in Caucasians.
  מאת: Owen, F, et al.
  יצא לאור: (1990)
• Panencephalopathic Creutzfeldt‐Jakob Disease with Distinct Pattern of Prion Protein Deposition in a Patient with D178N Mutation and Homozygosity for Valine at Codon 129 of the Prion Protein Gene
  מאת: Marcon, Gabriella, et al.
  יצא לאור: (2013)
• FATAL FAMILIAL INSOMNIA, A PRION DISEASE WITH A MUTATION AT CODON 178 OF THE PRION PROTEIN GENE
  מאת: Medori, Rossella, et al.
  יצא לאור: (1992)
• Familial fatal insomnia with atypical clinical features in a patient with D178N mutation and homozygosity for Met at codon 129 of the prion protein gene
  מאת: Sun, Lin, et al.
  יצא לאור: (2015)