2,8-Dihydroxyadenine urolithiasis due to partial deficit in adenine phosphoribosyltransferase : a case report
Inherited metabolic diseases resulting in urolithiasis secondary to urinary excretion of insoluble substances are rare but often present as urinary obstruction of renal insufficiency. We herein report a case of partial adenine phosphoribosyltransferase deficiency associated with 2,8-dihydroxyadenine...
| Publié dans: | Hinyokika kiyo. Acta urologica Japonica. - 1962. - 38(1992), 5 vom: 09. Mai, Seite 573-7 |
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| Auteur principal: | |
| Autres auteurs: | , , , |
| Format: | Article |
| Langue: | English |
| Publié: |
1992
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| Accès à la collection: | Hinyokika kiyo. Acta urologica Japonica |
| Sujets: | Case Reports Journal Article 2,8-dihydroxyadenine 30377-37-8 Adenine Phosphoribosyltransferase EC 2.4.2.7 Adenine JAC85A2161 |