References
Wright EM, Hirayama BA, Loo DF (2007) Active sugar transport in health and disease. J Intern Med 261:32–43
Santer R, Kinner M, Lassen CL et al (2003) Analysis of the SGLT2 gene in patients with renal glucosuria. J Am Soc Nephrol 14:2873–2882
Calado J, Loeffler J, Sakallioglu O et al (2006) Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting. Kidney Int 69:852–855
Calado J, Sznajer Y, Metzger D et al (2008) Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion. Nephrol Dial Transplant 23:3874–3879
Yu L, Lv JC, Zhou XJ et al (2011) Abnormal expression and dysfunction of novel SGLT2 mutations identified in familial renal glucosuria patients. Hum Genet 129:335–344
Acknowledgments
This work was funded by the National Natural Science Foundation of China (#81160087) and the Natural Science Fund of the Inner Mongolia Autonomous Region (#2010BS1102).
Conflict of interest
The authors declare that they have no conflict of interest.
Author information
Authors and Affiliations
Corresponding author
Additional information
L. Yu and P. Hou are co-first authors and have contributed equally to the work.
Rights and permissions
About this article
Cite this article
Yu, L., Hou, P., Lv, JC. et al. A novel sodium–glucose co-transporter 2 gene (SGLT2) mutation contributes to the abnormal expression of SGLT2 in renal tissues in familial renal glucosuria. Int Urol Nephrol 46, 2237–2238 (2014). https://doi.org/10.1007/s11255-014-0755-5
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11255-014-0755-5