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Mutations in Glucose Transporter 9 Gene SLC2A9 Cause Renal Hypouricemia
Renal hypouricemia is an inherited disorder characterized by impaired renal urate (uric acid) reabsorption and subsequent low serum urate levels, with severe complications such as exercise-induced acute renal failure and nephrolithiasis. We previously identified SLC22A12, also known as URAT1, as a c...
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| Main Authors: | , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2668068/ https://ncbi.nlm.nih.gov/pubmed/19026395 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2008.11.001 |
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