Associated Papers
A case of xanthinuria type I with a novel mutation in xanthine dehydrogenase.
Iguchi A et al.
Cen Case Reports, 2016
Depletion of Uric Acid Due to SLC22A12 (URAT1) Loss-of-Function Mutation Causes Endothelial Dysfunction in Hypouricemia.
Sugihara S et al.
Circulation Journal : Official Journal of the Japanese Circulation Society, 2015
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