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10.1038/nri1001 Nat

SLC22A12 gene encoding for the urate transporter hURAT1 defects leads to primary renal hypouricemia characterized by increased UA excretion from a reduced reabsorption ( SLC2A9 gene, encoding the urate transporter GLUT9, are closely related to human cognition and neurodegenerative diseases ( Urate Transporters and Genetics of Urate Transporter Pathologies A series of urate transporters including SLC and ABC transporters as well as several multispecific drug transporters (e.g., OAT1, OAT2, and ABCG2) maintain UA homeostasis (Figure 2) (Table 1)

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According to the note, the TGA has received reports of people experiencing severe inflammation, allergic reactions involving hospitalisation, blurred vision, muscle injuries and insomnia

Ma C, Wang Y, Zhang G, Dai X