Benign mitochondrial encephalomyopathy in a patient with complex I deficiency

J Inherit Metab Dis. 1996;19(2):149-52. doi: 10.1007/BF01799416.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Consanguinity
  • Female
  • Humans
  • Infant, Newborn
  • Mitochondrial Encephalomyopathies / etiology*
  • NAD(P)H Dehydrogenase (Quinone) / deficiency*

Substances

  • NAD(P)H Dehydrogenase (Quinone)