Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum

Mov Disord. 2008 Apr 30;23(6):917-9. doi: 10.1002/mds.21942.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Consanguinity
  • Corpus Callosum / pathology*
  • Female
  • Gait Disorders, Neurologic / genetics
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Mutation
  • Proteins / genetics*
  • Spastic Paraplegia, Hereditary / genetics*
  • Spastic Paraplegia, Hereditary / pathology*

Substances

  • Proteins
  • SPG11 protein, human