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Urinary organic acids in a case of congenital lactic acidosis due to pyruvate decarboxylase deficiency.

AuthorsR A Chalmers, A M Lawson, O Borud
JournalJournal of inherited metabolic disease (J Inherit Metab Dis) Vol. 1 Issue 1 Pg. 15-6 ( 1978) ISSN: 0141-8955 [Print] United States
PMID117229 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Carboxylic Acids
  • Ketoglutaric Acids
  • Lactates
  • Malates
  • Pyruvates
  • Succinates
  • Carboxy-Lyases
  • Pyruvate Decarboxylase
Topics
  • Carboxy-Lyases (deficiency)
  • Carboxylic Acids (urine)
  • Female
  • Humans
  • Infant, Newborn
  • Ketoglutaric Acids (urine)
  • Lactates (urine)
  • Malates (urine)
  • Pyruvate Decarboxylase (deficiency)
  • Pyruvates (urine)
  • Succinates (urine)

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