The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia (Q44822748)
scientific article published on 31 March 2004
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Current Data About The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia
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(P1476) "The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia" (language: en)
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(P2093) 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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other details
description scientific article published on 31 March 2004

External Links
(P356) 10.1007/S00467-004-1424-1
(P698) 15054642