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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,...
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| Publicado no: | Exp Ther Med |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
D.A. Spandidos
2016
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| Assuntos: | |
| Acesso em linha: | 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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