Creutzfeldt-Jakob disease in a young person with valine homozygosity at codon 129: sporadic or variant?

C E Hillier, J G Llewelyn, J W Neal, J W Ironside

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)134-5
Number of pages2
JournalJournal of Neurology, Neurosurgery & Psychiatry
Volume70
Issue number1
Publication statusPublished - Jan 2001

Keywords / Materials (for Non-textual outputs)

  • Adult
  • Codon
  • Creutzfeldt-Jakob Syndrome
  • Homozygote
  • Humans
  • Male
  • Valine

Cite this