SPG46 and SPG56 are rare causes of hereditary spastic paraplegia in China

J Neurol. 2016 Oct;263(10):2136-8. doi: 10.1007/s00415-016-8256-3. Epub 2016 Aug 23.
No abstract available

Publication types

  • Letter
  • Video-Audio Media

MeSH terms

  • Adolescent
  • Adult
  • China
  • Cohort Studies
  • Female
  • Glucosylceramidase
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Mutation / genetics*
  • Pedigree
  • Spastic Paraplegia, Hereditary / diagnostic imaging
  • Spastic Paraplegia, Hereditary / genetics*
  • Young Adult
  • beta-Glucosidase / genetics*

Substances

  • beta-Glucosidase
  • GBA2 protein, human
  • Glucosylceramidase