Deficiency in ubiquinone cytochrome c reductase in a patient with mitochondrial myopathy and lactic acidosis.

Lignende værker

• Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene
  af: Horvath, R, et al.
  Udgivet: (2002)
• Reversible mitochondrial myopathy with cytochrome c oxidase deficiency.
  af: Salo, M K, et al.
  Udgivet: (1992)
• Long-Standing Hypokalemia and Lactic Acidosis as the Primary Presentation of Mitochondrial Myopathy
  af: Miao, Jing, et al.
  Udgivet: (2020)
• Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis.
  af: Moreadith, R W, et al.
  Udgivet: (1984)
• Chronic lactic acidosis in association with myopathy.
  af: Terlow, M J, et al.
  Udgivet: (1973)