The W258X mutation in SLC22A is the predominant cause of Japanese renal hypouricemia.
Bibliographic Information
- Title
- The W258X mutation in SLC22A is the predominant cause of Japanese renal hypouricemia.
- Author
- komoda F, Igarashi T, et al.
Journal
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- Pediatr Nephrol 19(5)
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Pediatr Nephrol 19(5) 728-733, 2004
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Details 詳細情報について
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- CRID
- 1010282256862087827
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- Article Type
- journal article
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- Data Source
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- KAKEN