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Q36480292-7ABADCDE-B0C4-422F-9E66-E235F16D6920
Q36480292-7ABADCDE-B0C4-422F-9E66-E235F16D6920
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http://www.wikidata.org/entity/statement/Q36480292-7ABADCDE-B0C4-422F-9E66-E235F16D6920
Analysis of mutations in the urate transporter 1 (URAT1) gene of Japanese patients with hypouricemia in northern Japan and review of the literature.
P2860
Q36480292-7ABADCDE-B0C4-422F-9E66-E235F16D6920
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36480292-7ABADCDE-B0C4-422F-9E66-E235F16D6920
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wasDerivedFrom
c815189dc1c676857a2b0c904b25ed5b877c23bd
P2860
The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia.