Multiple molybdoenzyme deficiencies due to an inborn error of molybdenum cofactor metabolism: Two additional cases in a new family
- 1 June 1983
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 6 (S2) , 95-96
- https://doi.org/10.1007/bf01810344
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- 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
- Combined deficiency of xanthine oxidase and sulphite oxidase: A defect of molybdenum metabolism or transport?Journal of Inherited Metabolic Disease, 1978
- A colorimetric method for the determination of thiosulfateBiochimica et Biophysica Acta, 1957