Childhood hyperuricemia and acute renal failure resulting from a missense mutation in theHPRT gene
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference17 articles.
1. Partial Deficit of Hypoxanthine Guanine Phosphoribosyl Transferase Presenting as Acute Renal Failure
2. RENAL FAILURE IN INFANCY DUE TO OVER-PRODUCTION OF URATE
3. Gout, uric acid and purine metabolism in paediatric nephrology
4. 1997. Inherited disorders of purine metabolism and transport. In: editors. Oxford textbook of clinical nephrology. Oxford: Oxford University Press. p. 2469-2483.
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