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Amino acid profile in pyruvate carboxylase deficiency: Comparison with some other metabolic disorders

  • C. Charpentier
  • J. M. Tetau
  • H. Ogier
  • J. M. Saudubray
  • F. X. Coude
  • A. Lemonnier
Short Communication

Keywords

Public Health Internal Medicine Pyruvate Metabolic Disease Metabolic Disorder 
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. Carson, N. A. J., Scally, B. G., Neill, D. W. and Carre, I. J. Saccharopinuria: a new inborn error of lysine metabolism.Nature 218 (1968) 679Google Scholar
  2. Halperin, M. L., Schiller, C. M. and Fritz, I. B. The inhibition by methylmalonic acid of malate transport by the dicarboxylate carrier in rat liver mitochondria. A possible explanation for hypoglycemia in methylmalonic aciduria.J. Clin. Invest. 50 (1971) 2276–2280Google Scholar
  3. Przyrembel, H., Wendel, U., Becker, K., Bremer, H. J., Bruinvis, L., Ketting, D. and Wadman, S. K. Glutaric aciduria type II: report on a previously undescribed metabolic disorder.Clin. Chim. Acta 66 (1976) 227–239Google Scholar
  4. Sweetman, L., Nyhan, W. L., Trauner, D. A., Nerritt, T. A. and Singh, M. Glutaric aciduria type II.J. Pediatr. 96 (1980) 1020–1026Google Scholar

Copyright information

© MTP Press Limited 1982

Authors and Affiliations

  • C. Charpentier
    • 1
    • 2
  • J. M. Tetau
    • 1
    • 2
  • H. Ogier
    • 1
    • 2
  • J. M. Saudubray
    • 1
    • 2
  • F. X. Coude
    • 1
    • 2
  • A. Lemonnier
    • 1
    • 2
  1. 1.Laboratoire de BiochimieKremlin-BicetreFrance
  2. 2.Service de Génétique du Pr Frezal, CHU NeckerParisFrance

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