The expanding neurological phenotype of DNM1L-related disorders

Brain. 2018 Apr 1;141(4):e28. doi: 10.1093/brain/awy024.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • GTP Phosphohydrolases / genetics
  • Humans
  • Microtubule-Associated Proteins / genetics
  • Mitochondrial Dynamics*
  • Mitochondrial Proteins
  • Mutation
  • Optic Atrophy, Autosomal Dominant*
  • Phenotype

Substances

  • Microtubule-Associated Proteins
  • Mitochondrial Proteins
  • GTP Phosphohydrolases
  • OPA1 protein, human
  • DNM1L protein, human