Expanding the clinical spectrum of myopathy, encephalopathy, lactic acidosis, and stroke-like (MELAS) episode: A case with A3243G mitochondrial DNA mutation presenting as MELAS and congenital melanocytic naevi overlap

Neurol India. 2016 Mar-Apr;64(2):336-8. doi: 10.4103/0028-3886.177607.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • DNA, Mitochondrial / genetics*
  • Humans
  • MELAS Syndrome / genetics*
  • Mutation*
  • Nevus, Pigmented / genetics*

Substances

  • DNA, Mitochondrial