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SLC5A2 mutations, including two novel mutations, responsible for renal glucosuria in Chinese families
BACKGROUND: Familial renal glucosuria (FRG) is characterized by persistent glucosuria without other impairments of tubular function in the presence of normal serum glucose. SGLT2, which is almost exclusively expressed in the kidney, accounts for most of the glucose reabsorption. Recently, some studi...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7047355/ https://www.ncbi.nlm.nih.gov/pubmed/32111189 http://dx.doi.org/10.1186/s12882-020-01725-9 |