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Journal of Inherited Metabolic Disease

, Volume 19, Issue 6, pp 793–794 | Cite as

Persistent glycolic aciduria in a healthy child with normal alanine-glyoxylate aminotransferase activity

  • W. J. Craigen
Case Report

Keywords

Public Health Internal Medicine Metabolic Disease Healthy Child Aminotransferase Activity 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Danpure C, Purdue PE (1995) Primary hyperoxaluria. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds.The Metabolic and Molecular Bases of Inherited Disease, 7th edn, New York: McGraw-Hill, 945–961.Google Scholar
  2. Fry DW, Richardson KE (1979a) Isolation and characterization of glycolic acid oxidase from human liver.Biochim Biophys Acta 568: 135–144.Google Scholar
  3. Fry DW, Richardson KE (1979b) Isolation and characterization of glycolic acid dehydrogenase from human liver.Biochim Biophys Acta 567: 482–491.Google Scholar
  4. Jakobs C, Jaeken J, Gibson KM (1993) Inherited disorders of GABA metabolism.J Inher Metab Dis 16: 705–715.Google Scholar

Copyright information

© SSIEM and Kluwer Academic Publishers 1996

Authors and Affiliations

  • W. J. Craigen
    • 1
  1. 1.Departments of Molecular and Human Genetics and PediatricsBaylor College of Medicine, One Baylor PlazaHoustonUSA

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