Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation

Ann Neurol. 2004 Dec;56(6):909-10; author reply 910-1. doi: 10.1002/ana.20327.
No abstract available

Publication types

  • Comment
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asparagine / genetics
  • Aspartic Acid / genetics
  • Brain / pathology
  • Humans
  • Mutation*
  • PrPSc Proteins / genetics*
  • Prion Diseases / genetics*
  • Prion Diseases / pathology

Substances

  • PrPSc Proteins
  • Aspartic Acid
  • Asparagine