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Mutations associated with functional disorder of xanthine oxidoreductase and hereditary xanthinuria in humans |
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| | Ichida, K. and Amaya, Y. and Okamoto, K. and Nishino, T. | | | International Journal of Molecular Sciences. 2012; 13(11): 15475-15495 | | | [Pubmed] [Google Scholar] | | 2 |
Pediatric urolithiasis: Causative factors, diagnosis and medical management |
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