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Hypouricaemia and hyperuricosuria in familial renal glucosuria
Familial renal glucosuria is a rare co-dominantly inherited benign phenotype characterized by the presence of glucose in the urine. It is caused by mutations in the SLC5A2 gene that encodes SGLT2, the Na(+)-glucose cotransporter responsible for the reabsorption of the bulk of glucose in the proximal...
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| Udgivet i: | Clin Kidney J |
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| Main Authors: | , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Oxford University Press
2013
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4438413/ https://ncbi.nlm.nih.gov/pubmed/26064518 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/ckj/sft100 |
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