Prion codon 129 homozygosity and sporadic inclusion body myositis

Neurology. 2001 Jul 24;57(2):368. doi: 10.1212/wnl.57.2.368.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Genotype
  • Homozygote
  • Humans
  • Myositis, Inclusion Body / genetics*