The W258X mutation in SLC22A is the predominant cause of Japanese renal hypouricemia.
書誌事項
- タイトル
- The W258X mutation in SLC22A is the predominant cause of Japanese renal hypouricemia.
- 著者
- komoda F, Igarashi T, et al.
収録刊行物
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- Pediatr Nephrol 19(5)
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Pediatr Nephrol 19(5) 728-733, 2004