Hereditary renal hypouricemia. Isolated tubular defect of urate reabsorption
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference20 articles.
1. Inborn hypouricemia due to isolated renal tubular defect;De Vries;Biomedicine,1979
2. Uric acid in two patients with Wilson's disease (hepatolenticular degeneration);Bishop;Proc Soc Exp Biol med,1954
3. Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal aminoaciduria and other bizarre biochemical features;Baron;Lancet,1956
4. The adult Fanconi syndrome. II. Review of eighteen cases;Wallis;Am J Med,1957
5. Familial hypouricemia due to isolated renal tubular defect;Benjamin;Nephron,1977
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