A Recurrent KPNA3 Missense Variant Causing Infantile Pure Spastic Paraplegia

Ann Neurol. 2022 Feb;91(2):298-299. doi: 10.1002/ana.26297. Epub 2022 Jan 20.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Humans
  • Mutation, Missense / genetics
  • Paraplegia
  • Spastic Paraplegia, Hereditary*
  • alpha Karyopherins

Substances

  • KPNA3 protein, human
  • alpha Karyopherins