'Behr syndrome' with OPA1 compound heterozygote mutations

Brain. 2015 Jan;138(Pt 1):e321. doi: 10.1093/brain/awu234. Epub 2014 Aug 21.
No abstract available

Publication types

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

MeSH terms

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

Substances

  • GTP Phosphohydrolases