Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleURAT1 mutations cause renal hypouricaemia combined with Fanconi syndrome in a Chinese patient.AuthorsDu, Juan; Jiang, Yan; Wang, Ou; Li, Mei; Xing, Xiao‐Ping; Xia, WeiboSubjectsKIDNEY tubules; FANCONI syndromePublicationNephrology, 2018, Vol 23, Issue 8, p797ISSN1320-5358Publication typeLetter to the EditorDOI10.1111/nep.13190