A family of hereditary xanthinuria: two siblings with peptic ulcer and hypouricemia due to xanthine oxidase deficiency, and a heterozygote (father) with gout

M. Kawachi*, N. Kono, I. Mineo, N. Hara, Y. Yamada, H. Kiyokawa, S. Himeno, S. Tarui, T. Miyazaki

*Corresponding author for this work

Research output: Contribution to journalArticle

2 Scopus citations
Original languageEnglish (US)
Pages (from-to)47-52
Number of pages6
JournalNihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine
Volume77
Issue number1
DOIs
StatePublished - Jan 1988

ASJC Scopus subject areas

  • Medicine(all)

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