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Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia. [electronic resource] by
- Wakida, Naoki
- Tuyen, Do Gia
- Adachi, Masataka
- Miyoshi, Taku
- Nonoguchi, Hiroshi
- Oka, Toshiaki
- Ueda, Osamu
- Tazawa, Masahiro
- Kurihara, Satoshi
- Yoneta, Yoshitaka
- Shimada, Hajime
- Oda, Takashi
- Kikuchi, Yuichi
- Matsuo, Hirotaka
- Hosoyamada, Makoto
- Endou, Hitoshi
- Otagiri, Masaki
- Tomita, Kimio
- Kitamura, Kenichiro
Producer: 20050531
In:
The Journal of clinical endocrinology and metabolism vol. 90
Availability: No items available.
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