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

مواد مشابهة

• Prion protein gene analysis in three kindreds with fatal familial insomnia (FFI): codon 178 mutation and codon 129 polymorphism.
  بواسطة: Medori, R, وآخرون
  منشور في: (1993)
• FATAL FAMILIAL INSOMNIA, A PRION DISEASE WITH A MUTATION AT CODON 178 OF THE PRION PROTEIN GENE
  بواسطة: Medori, Rossella, وآخرون
  منشور في: (1992)
• Clinical Features of Fatal Familial Insomnia: Phenotypic Variability in Relation to a Polymorphism at Codon 129 of the Prion Protein Gene
  بواسطة: Montagna, Pasquale, وآخرون
  منشور في: (2006)
• Medical genetics: advances in brief: Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene
  بواسطة: Norman, A M
  منشور في: (1992)
• 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
  بواسطة: Marcon, Gabriella, وآخرون
  منشور في: (2013)