Molybdenum cofactor deficiency in a patient previously characterized as deficient in sulfite oxidase
- 1 August 1988
- journal article
- research article
- Published by Elsevier in Biochemical Medicine and Metabolic Biology
- Vol. 40 (1) , 86-93
- https://doi.org/10.1016/0885-4505(88)90108-9
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- In vitro reconstitution of nitrate reductase activity of the Neurospora crassa mutant nit-1: Specific incorporation of molybdopterinArchives of Biochemistry and Biophysics, 1984
- Separation and quantitation of oxypurines by isocratic high-pressure liquid chromatography: Application to xanthinuria and the Lesch-Nyhan syndromeBiochemical Medicine, 1983
- Absence of hepatic molybdenum cofactor: An inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenaseJournal of Inherited Metabolic Disease, 1983
- Inborn errors of molybdenum metabolism: combined deficiencies of sulfite oxidase and xanthine dehydrogenase in a patient lacking the molybdenum cofactor.Proceedings of the National Academy of Sciences, 1980
- Characterization of the molybdenum cofactor of sulfite oxidase, xanthine, oxidase, and nitrate reductase. Identification of a pteridine as a structural component.Journal of Biological Chemistry, 1980
- Characterization of molybdenum cofactor from Escherichia coliJournal of Bacteriology, 1979
- Sulfite Oxidase DeficiencyNew England Journal of Medicine, 1977
- Human sulfite oxidase deficiency. Characterization of the molecular defect in a multicomponent system.Journal of Clinical Investigation, 1976
- Sulfite oxidase deficiency: Studies of a patient with mental retardation, dislocated ocular lenses, and abnormal urinary excretion of S-sulfo-l-cysteine, sulfite, and thiosulfateBiochemical Medicine, 1967
- Sulfite Oxidase Deficiency in Man: Demonstration of the Enzymatic DefectScience, 1967