The X-chromosomal NDUFA1 gene of complex I in mitochondrial encephalomyopathies: tissue expression and mutation detection

J Inherit Metab Dis. 1998 Jun;21(3):210-5. doi: 10.1023/a:1005339332062.
No abstract available

MeSH terms

  • DNA, Complementary
  • Electron Transport Complex I
  • Female
  • Humans
  • Male
  • Mitochondrial Encephalomyopathies / genetics*
  • Mitochondrial Encephalomyopathies / metabolism
  • Mutation*
  • NAD(P)H Dehydrogenase (Quinone) / genetics*
  • NAD(P)H Dehydrogenase (Quinone) / metabolism
  • NADH, NADPH Oxidoreductases / genetics*
  • NADH, NADPH Oxidoreductases / metabolism
  • RNA, Messenger
  • Tissue Distribution
  • X Chromosome*

Substances

  • DNA, Complementary
  • RNA, Messenger
  • NADH, NADPH Oxidoreductases
  • NAD(P)H Dehydrogenase (Quinone)
  • Electron Transport Complex I