Biotin-dependent Carboxylase Deficiencies (Propionyl-CoA and Pyruvate Carboxylases)
- 1 June 1985
- journal article
- Published by Wiley in Annals of the New York Academy of Sciences
- Vol. 447 (1 Biotin) , 225-234
- https://doi.org/10.1111/j.1749-6632.1985.tb18441.x
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Sheep Liver Propionyl-CoA Carboxylase: Purification and Some Molecular PropertiesAnnals of the New York Academy of Sciences, 1985
- Amino acid profile in pyruvate carboxylase deficiency: Comparison with some other metabolic disordersJournal of Inherited Metabolic Disease, 1982
- Lactic acidosis due to pyruvate carboxylase deficiencyJournal of Inherited Metabolic Disease, 1981
- The Genetic Heterogeneity of Lactic Acidosis: Occurrence of Recognizable Inborn Errors of Metabolism in a Pediatric Population with Lactic AcidosisPediatric Research, 1980
- Purification of human liver propionyl-CoA carboxylase by carbon tetrachloride extraction and monomeric avidin affinity chromatographyArchives of Biochemistry and Biophysics, 1980
- Molecular basis for genetic complementation in propionyl CoA carboxylase deficiencyExperimental Cell Research, 1980
- Biotin-response OrganicaciduriaJournal of Clinical Investigation, 1979
- Asymptomatic propionyl CoA carboxylase deficiency in a 13-year-old girlThe Journal of Pediatrics, 1979
- Pyruvate Carboxylase Deficiency and Lactic Acidosis in a Retarded Child without Leigh's DiseasePediatric Research, 1979
- Pyruvate Carboxylase and Phosphoenolpyruvate Carboxykinase Activity in Leukocytes and Fibroblasts from a Patient with Pyruvate Carboxylase DeficiencyPediatric Research, 1979