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[Uncommon purine lithiasis: adenine phosphoribosyltransferase (APRT) deficiency and hereditary xanthinuria].

AuthorsJuan Antonio Orts Costa, Angel Zúñiga Cabrera, Susana Ferrando Monleón
JournalMedicina clinica (Med Clin (Barc)) Vol. 119 Issue 13 Pg. 508-15 (Oct 19 2002) ISSN: 0025-7753 [Print] Spain
Vernacular TitleLitiasis purínicas infrecuentes: déficit de adenina fosforribosiltransferasa y xantinuria hereditaria.
PMID12406401 (Publication Type: Journal Article, Review)
Chemical References
  • Xanthine Dehydrogenase
  • Adenine Phosphoribosyltransferase
Topics
  • Adenine Phosphoribosyltransferase (deficiency, genetics)
  • Gene Expression Regulation, Enzymologic
  • Genotype
  • Humans
  • Lithiasis (diagnosis, enzymology, etiology)
  • Phenotype
  • Xanthine Dehydrogenase (deficiency, genetics)

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