The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia (Q44822748)
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scientific article published on 31 March 2004
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia |
scientific article published on 31 March 2004 |
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The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia (English)
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Fusako Komoda
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Takashi Sekine
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Jun Inatomi
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Atsushi Enomoto
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Hitoshi Endou
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Toshiyuki Ota
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Takeshi Matsuyama
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Tsutomu Ogata
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Masahiro Ikeda
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Midori Awazu
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Isamu Kamimaki
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Takashi Igarashi
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31 March 2004
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728-733
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