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...

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Detalles Bibliográficos
Autores principales: Hakoda, Masayuki, Ichida, Kimiyoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313227/
https://www.ncbi.nlm.nih.gov/pubmed/35885001
http://dx.doi.org/10.3390/biomedicines10071696

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