Methionine homozygosity at prion gene codon 129 may predispose to sporadic inclusion-body myositis

Lancet. 1999 Feb 6;353(9151):465-6. doi: 10.1016/S0140-6736(98)05208-8.
No abstract available

Publication types

  • Letter

MeSH terms

  • Codon / genetics*
  • Genetic Predisposition to Disease*
  • Homozygote
  • Humans
  • Methionine / genetics*
  • Middle Aged
  • Myositis, Inclusion Body / genetics*
  • Prions / genetics*

Substances

  • Codon
  • Prions
  • Methionine