Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation

Brain. 2011 Nov;134(Pt 11):e195. doi: 10.1093/brain/awr101. Epub 2011 Jun 6.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Central Nervous System Diseases / complications*
  • Female
  • GTP Phosphohydrolases / genetics*
  • Humans
  • Male
  • Optic Atrophy, Autosomal Dominant / complications*

Substances

  • GTP Phosphohydrolases