Concepedia

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The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia

DOI

82

Citations

12

References

2004

Year

Fusako Komoda, Takashi Sekine, Jun Inatomi, Atsushi Enomoto, Hitoshi Endou, Toshiyuki Ota, Takeshi Matsuyama, Tsutomu Ogata, Masahiro Ikeda, Midori Awazu,
Pediatric Nephrology

References

YearCitations

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