Diversity in residual alanine glyoxylate aminotransferase activity in hyperoxaluria type I: Correlation with pyridoxine responsiveness
- 1 June 1988
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 11 (S2) , 208-211
- https://doi.org/10.1007/bf01804237
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndromeClinica Chimica Acta; International Journal of Clinical Chemistry, 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
- Glycolate and Glyoxylate Metabolism by Isolated Peroxisomes or ChloroplastsPlant Physiology, 1969