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Diversity in residual alanine glyoxylate aminotransferase activity in hyperoxaluria type I: Correlation with pyridoxine responsiveness

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References

  1. Danpure, C. J. and Jennings, P. R. Peroxisomal alanine glyoxylate aminotransferase deficiency in primary hyperoxaluria type I.FEBS Lett. 201 (1986) 20–24

  2. Danpure, C. J., Jennings, P. R. and Watts, R. W. E. Enzymological diagnosis of primary hyperoxaluria type I by measurement of hepatic alanine: glyoxylate aminotransferase activity.Lancet 1 (1987) 289–291

  3. Kisaki, T. and Tolbert, N. E. Glycolate and glyoxylate metabolism by isolated peroxisomes and chloroplasts.Plant Physiol. 44 (1969) 242–250

  4. Wanders, R. J. A., van Roermund, C. W. T., Westra, R., Schutgens, R. B. H., van der Ende, M. A., Tager, J. M., Monnens, L. A. H., Baadenhuysen, H., Govaerts, L., Przyrembel, H., Wolff, H., Blom, W., Huymans, J. G. M. and van Laarhoven, F. G. M. Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycolate in hyperoxaluria type I and the Zellweger syndrome.Clin. Chim. Acta 165 (1987) 311–319

  5. Williams, H. E. and Smith, L. H. Primary hyperoxaluria. In Stanbury, J. B., Wyngaarden, J. B., Fredrickson, D. S., Goldstein, J. L. and Brown, M. S., eds.The Metabolic Basis of Inherited Disease, 5th Edition, McGraw-Hill, New York, 1983, pp. 204–228

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Wanders, R.J.A., van Roermund, C.W.T., Jurriaans, S. et al. Diversity in residual alanine glyoxylate aminotransferase activity in hyperoxaluria type I: Correlation with pyridoxine responsiveness. J Inherit Metab Dis 11, 208–211 (1988). https://doi.org/10.1007/BF01804237

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Keywords

  • Public Health
  • Internal Medicine
  • Alanine
  • Metabolic Disease
  • Pyridoxine