Uncommon phenotype for a codon 178 mutation of the human PrP gene

Ann Neurol. 1992 Mar;31(3):345. doi: 10.1002/ana.410310321.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Age Factors
  • Codon
  • Creutzfeldt-Jakob Syndrome / genetics*
  • Genes
  • Genetic Predisposition to Disease
  • Humans
  • Male
  • Middle Aged
  • Mutation
  • Pedigree
  • Phenotype
  • PrPC Proteins
  • Prions / genetics*
  • Protein Precursors / genetics*

Substances

  • Codon
  • PrPC Proteins
  • Prions
  • Protein Precursors