Gerstmann-Straussler-Scheinker disease due to a novel prion protein gene mutation

Neurology. 2011 Feb 1;76(5):485-7. doi: 10.1212/WNL.0b013e31820a0ab2.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Atrophy
  • Diagnosis, Differential
  • Genetic Predisposition to Disease / genetics
  • Gerstmann-Straussler-Scheinker Disease / diagnosis
  • Gerstmann-Straussler-Scheinker Disease / genetics*
  • Gerstmann-Straussler-Scheinker Disease / pathology
  • Humans
  • Male
  • Mutation / genetics*
  • Prion Diseases / diagnosis
  • Prion Diseases / genetics*
  • Prion Diseases / pathology
  • Prion Proteins
  • Prions / genetics*

Substances

  • PRNP protein, human
  • Prion Proteins
  • Prions