Familial mitochondrial complex I deficiency with an abnormal mitochondrial encoded protein

J Inherit Metab Dis. 1989:12 Suppl 2:355-7. doi: 10.1007/BF03335421.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Cells, Cultured
  • DNA, Mitochondrial / genetics*
  • Humans
  • Infant, Newborn
  • Male
  • Mitochondria, Muscle / enzymology*
  • Molecular Weight
  • NAD(P)H Dehydrogenase (Quinone)
  • Quinone Reductases / deficiency*
  • Quinone Reductases / genetics
  • Quinone Reductases / isolation & purification

Substances

  • DNA, Mitochondrial
  • NAD(P)H Dehydrogenase (Quinone)
  • Quinone Reductases