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Human Mutations in SLC2A9 (Glut9) Affect Transport Capacity for Urate

SLC2A9 or Glut9 is a voltage sensitive urate transporter, mainly expressed in the kidneys, the liver, and the intestine. Human Glut9 loss-of-function mutations were identified in familial hypouricemia, and several single nucleotide polymorphisms (SNPs) were associated with lower serum urate, further...

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Detalles Bibliográficos
Autores principales: Ruiz, Anne, Gautschi, Ivan, Schild, Laurent, Bonny, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016318/
https://www.ncbi.nlm.nih.gov/pubmed/29967582
http://dx.doi.org/10.3389/fphys.2018.00476

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