Enzymatic heterogeneity in primary hyperoxaluria type 1 (hepatic peroxisomal alanine: Glyoxylate aminotransferase deficiency)
- 1 June 1988
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 11 (S2) , 205-207
- https://doi.org/10.1007/bf01804236
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- A new micro-assay for human liver alanine : Glyoxylate aminotransferaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1987
- Immunological heterogeneity of hepatic alanine:glyoxylate aminotransferase in primary hyperoxaluria type 1FEBS Letters, 1987
- ENZYMOLOGICAL DIAGNOSIS OF PRIMARY HYPEROXALURIA TYPE 1 BY MEASUREMENT OF HEPATIC ALANINE: GLYOXYLATE AMINOTRANSFERASE ACTIVITYThe Lancet, 1987
- Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type IFEBS Letters, 1986
- Mitochondrial damage and the subcellular distribution of 2-oxoglutarate:glyoxylate carboligase in normal human and rat liver and in the liver of a patient with primary hyperoxaluria type IClinical Science, 1986
- Assays for glyoxylate aminotransferase activitiesInternational Journal of Biochemistry, 1972
- Isolation and characterization of a glutamate-glycine transaminase from human liverArchives of Biochemistry and Biophysics, 1966