Mutations in Glucose Transporter 9 Gene SLC2A9 Cause Renal Hypouricemia

Author:

Matsuo Hirotaka,Chiba Toshinori,Nagamori Shushi,Nakayama Akiyoshi,Domoto Hideharu,Phetdee Kanokporn,Wiriyasermkul Pattama,Kikuchi Yuichi,Oda Takashi,Nishiyama Junichiro,Nakamura Takahiro,Morimoto Yuji,Kamakura Keiko,Sakurai Yutaka,Nonoyama Shigeaki,Kanai Yoshikatsu,Shinomiya Nariyoshi

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference27 articles.

1. Patients with renal hypouricemia with exercise-induced acute renal failure and chronic renal dysfunction;Kikuchi;Clin. Nephrol.,2000

2. Evidence for a postsecretory reabsorptive site for uric acid in man;Diamond;J. Clin. Invest.,1973

3. Molecular identification of a renal urate anion exchanger that regulates blood urate levels;Enomoto;Nature,2002

4. Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia;Wakida;J. Clin. Endocrinol. Metab.,2005

5. Clinical and molecular analysis of patients with renal hypouricemia in Japan-influence of URAT1 gene on urinary urate excretion;Ichida;J. Am. Soc. Nephrol.,2004

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