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Novel SLC5A2 mutation contributes to familial renal glucosuria: Abnormal expression in renal tissues

Familial renal glucosuria (FRG) is characterized by persistent glucosuria in the presence of normal serum glucose concentrations, while other impairments of tubular function are absent. Mutations in the sodium-glucose co-transporter 2 (SLC5A2) gene have been found to be responsible for FRG. However,...

詳細記述

保存先:
書誌詳細
出版年:Exp Ther Med
主要な著者: Yu, Lei, Hou, Ping, Liu, Guo-Ping, Zhang, Hong
フォーマット: Artigo
言語:Inglês
出版事項: D.A. Spandidos 2016
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4950299/
https://ncbi.nlm.nih.gov/pubmed/27446256
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2016.3388
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