TRMT5 mutations are associated with features of complex hereditary spastic paraparesis

Neurology. 2017 Nov 21;89(21):2210-2211. doi: 10.1212/WNL.0000000000004657. Epub 2017 Oct 11.
No abstract available

Publication types

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

MeSH terms

  • Female
  • Humans
  • Middle Aged
  • Paraparesis, Spastic / genetics*
  • Paraparesis, Spastic / physiopathology*
  • Siblings
  • Spastic Paraplegia, Hereditary / genetics*
  • Spastic Paraplegia, Hereditary / physiopathology*
  • tRNA Methyltransferases / genetics*

Substances

  • tRNA Methyltransferases
  • TRMT5 protein, human