2Enomoto A, Niwa T, Kanai Y, et al. Urate transporter and renal hypouricemia Rinsho Byori, 2003,51:892-897.
3Hediger MA. Physiology and biochemistry of uric acid. Ther Umsch,2004,61:541-545.
4Ichida K, Hosoyamada M, Hisatome I, et al. Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion. J Am Soc Nephrol, 2004,15: 164-173.
5Leal-Pinto E, Cohen BE, Lipkowitz MS, et al. Functional analysisand molecular model of the human urate transporter/channel, hUAT. Am J Physiol Renal Physiol, 2002,283:150-163.
6Lipkowitz MS, Leal-Pinto E, Cohen BE, et al. Galectin 9 is the sugarregulated urate transporter/channel UAT. Glycoconj J, 2004,19:491-498.
7Hyink DP, Rappoport JZ, Wilson PD, et al. Expression of the urate transporter/channel is developmentally regulated in human kidneys. Am J Physiol Renal Physiol, 2001,281: 875-886.
8Lipkowitz MS, Leal-Pinto E, Rappoport JZ, et al. Functional reconstitution, membrane targeting, genomic structure, and chromosomal localization of a human urate transporter. J Clin Invest, 2001,107:1103-1115.
9Yamada Y. Complete and partial deficiencies of hypoxanthine guanine phosphoribosyltransferase (HPRT). Nippon Rinsho, 2003, 61: 288-293.
10Mak BS, Chi CS, Tsai CR, et al. New mutations of the HPRT gene in Leseh-Nyhan syndrome. Pediatr Neurol, 2000,23:332-335.
