A novel mutation in SLC25A46 causes optic atrophy and progressive limb spasticity, with no cerebellar atrophy or axonal neuropathy

Clin Genet. 2017 Aug;92(2):230-231. doi: 10.1111/cge.12963. Epub 2017 Mar 30.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • DNA Mutational Analysis
  • Female
  • Humans
  • Male
  • Mitochondrial Proteins / genetics*
  • Mitochondrial Proteins / metabolism
  • Models, Molecular
  • Mutation*
  • Optic Atrophy / genetics*
  • Optic Atrophy / metabolism
  • Pedigree
  • Phosphate Transport Proteins / genetics*
  • Phosphate Transport Proteins / metabolism
  • Protein Conformation

Substances

  • Mitochondrial Proteins
  • Phosphate Transport Proteins
  • SLC25A46 protein, human