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Genetic Basis of the Epidemiological Features and Clinical Significance of Renal Hypouricemia
A genetic defect in urate transporter 1 (URAT1) is the major cause of renal hypouricemia (RHUC). Although RHUC is detected using a serum uric acid (UA) concentration <2.0 mg/dL, the relationship between the genetic state of URAT1 and serum UA concentration is not clear. Homozygosity and compound...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313227/ https://www.ncbi.nlm.nih.gov/pubmed/35885001 http://dx.doi.org/10.3390/biomedicines10071696 |