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The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia
Fusako Komoda, Takashi Sekine, Jun Inatomi, Atsushi Enomoto, Hitoshi Endou, Toshiyuki Ota, Takeshi Matsuyama, Tsutomu Ogata, Masahiro Ikeda, Midori Awazu, Koji Muroya, Isamu Kamimaki, Takashi Igarashi
Research output: Contribution to journal › Article › peer-review
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(Scopus)