MELAS/Leigh overlap syndrome due to the ND6 mutation m.10158T>C

Brain Dev. 2017 Sep;39(8):724. doi: 10.1016/j.braindev.2017.04.016. Epub 2017 May 15.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • DNA, Mitochondrial
  • Humans
  • Leigh Disease
  • MELAS Syndrome*
  • Mutation
  • Undifferentiated Connective Tissue Diseases*

Substances

  • DNA, Mitochondrial