Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia.

No abstract is available for this paper.

• Publication year

  2005

• Venue

  Journal of Clinical Endocrinology and Metabolism

• Publication date

  2005-04-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1210/JC.2004-1111PMID 15634722
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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

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