The W258X mutation in SLC22A is the predominant cause of Japanese renal hypouricemia.

Bibliographic Information

Title
The W258X mutation in SLC22A is the predominant cause of Japanese renal hypouricemia.
Author
komoda F, Igarashi T, et al.

Journal

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Details 詳細情報について

  • CRID
    1010282256862087827
  • Article Type
    journal article
  • Data Source
    • KAKEN

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