Diagnosing MELAS requires not only an mtDNA variant but also an appropriate phenotype

Doc Ophthalmol. 2019 Jun;138(3):255-256. doi: 10.1007/s10633-019-09690-x. Epub 2019 Mar 28.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • DNA, Mitochondrial
  • Electroretinography
  • Humans
  • MELAS Syndrome / genetics*
  • Phenotype
  • Retinal Dystrophies*
  • Sequence Deletion

Substances

  • DNA, Mitochondrial