Xanthinuria type I with a novel mutation of xanthine dehydrogenase

Am J Med Sci. 2015 Aug;350(2):155-6. doi: 10.1097/MAJ.0000000000000498.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Humans
  • Male
  • Metabolism, Inborn Errors / enzymology
  • Metabolism, Inborn Errors / genetics*
  • Middle Aged
  • Mutation*
  • Xanthine Dehydrogenase / deficiency*
  • Xanthine Dehydrogenase / genetics*

Substances

  • Xanthine Dehydrogenase

Supplementary concepts

  • Xanthinuria, Type I