URAT1 mutations cause renal hypouricaemia combined with Fanconi syndrome in a Chinese patient.
作者信息
Du Juan, Jiang Yan, Wang Ou, Li Mei, Xing Xiao-Ping, Xia Weibo
机构信息
Department of Endocrinology, Key Laboratory of Endocrinology, Ministry of Health, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
出版信息
Nephrology (Carlton). 2018 Aug;23(8):797-798. doi: 10.1111/nep.13190.
PMID:30920107
Abstract
摘要
Zotero 插件