A novel SGLT2 mutation in a patient with autosomal recessive renal glucosuria
Author:
Publisher
Oxford University Press (OUP)
Subject
Transplantation,Nephrology
Link
http://academic.oup.com/ndt/article-pdf/19/11/2893/5118794/gfh426.pdf
Cited by 38 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. High glucose–induced Smad3 linker phosphorylation and CCN2 expression are inhibited by dapagliflozin in a diabetic tubule epithelial cell model;Bioscience Reports;2021-06
2. Turning Foes to Friends: Knocking Down Diabetes Associated SGLT2 Transporters and Sustaining Life;Current Diabetes Reviews;2020-07-23
3. SLC5A2 mutations, including two novel mutations, responsible for renal glucosuria in Chinese families;BMC Nephrology;2020-02-28
4. Learning Physiology from Inherited Kidney Disorders;Physiological Reviews;2019-07-01
5. A novel compound heterozygous mutation in SLC5A2 contributes to familial renal glucosuria in a Chinese family, and a review of the relevant literature;Molecular Medicine Reports;2019-04-01
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