Creutzfeldt-Jakob disease in a heterozygous GBA mutation carrier: Coincidence or consequence?

Neurologia (Engl Ed). 2024 Sep;39(7):614-616. doi: 10.1016/j.nrleng.2024.07.005.
No abstract available

Publication types

  • Letter
  • Case Reports

MeSH terms

  • Creutzfeldt-Jakob Syndrome* / genetics
  • Female
  • Glucosylceramidase* / genetics
  • Heterozygote*
  • Humans
  • Male
  • Middle Aged
  • Mutation*

Substances

  • Glucosylceramidase
  • GBA protein, human