Commentary: New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the MT-ND4 Gene (m.12015T>C; p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2

Front Immunol. 2019 Jun 21;10:1333. doi: 10.3389/fimmu.2019.01333. eCollection 2019.
No abstract available

Keywords: MELAS; heteroplasmy; mtDNA; oxidative phosphorylation; stroke-like episode.

Publication types

  • Comment

MeSH terms

  • DNA, Mitochondrial
  • Diabetes Mellitus, Type 2*
  • Genes, Mitochondrial
  • Humans
  • MELAS Syndrome / genetics*
  • Point Mutation


  • DNA, Mitochondrial