Pathogenicity of the Homoplasmic m.8701A>G Variant Requires Confirmation

Chin Med J (Engl). 2016 Aug 5;129(15):1889-90. doi: 10.4103/0366-6999.186655.
No abstract available

Publication types

  • Letter

MeSH terms

  • Cardiomyopathy, Dilated / genetics
  • DNA, Mitochondrial / genetics
  • Humans
  • Hypertension / genetics
  • Mitochondrial Diseases / genetics
  • Mitochondrial Proton-Translocating ATPases / genetics*
  • Point Mutation / genetics

Substances

  • DNA, Mitochondrial
  • MT-ATP6 protein, human
  • Mitochondrial Proton-Translocating ATPases