Associated Papers
Structural basis of urate transport by glucose transporter 9.
Matsushita D et al.
Cell Reports, 2025
Biochemical characterization of renal hypouricemia-associated mutations in urate transporter genes using human cells.
Toyoda Y et al.
Human Cell, 2024
Raised CK and acute kidney injury following intense exercise in three patients with a history of exercise intolerance due to homozygous mutations in SLC2A9.
Quinlivan R et al.
Neuromuscular Disorders : Nmd, 2024
Recurrent exercise-induced acute kidney injury associated with hypouricemia: a case report and literature review.
Zhou J et al.
Bmc Nephrology, 2023
New SLC22A12 (URAT1) Variant Associated with Renal Hypouricemia Identified by Whole-Exome Sequencing Analysis and Bioinformatics Predictions.
Perdomo-Ramírez A et al.
Genes, 2023
Autosomal Recessive Renal Hypouricemia Type 2 Presenting with Childhood Stroke in a Sri Lankan Child.
Fernando PMS et al.
Laboratory Medicine, 2023
Exome sequencing and analysis of 454,787 UK Biobank participants.
Backman JD et al.
Nature, 2021
34662886 (PubMed )
Supplement: 41586_2021_4103_MOESM5_ESM.xlsx › SD3
Mutation in the SLC2A9 Gene: A New Family with Familial Renal Hypouricemia Type 2.
Maalouli C et al.
Case Reports in Nephrology, 2021
Human Mutations in SLC2A9 (Glut9) Affect Transport Capacity for Urate.
Ruiz A et al.
Frontiers in Physiology, 2018
Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2.
Mancikova A et al.
Clinical and Experimental Nephrology, 2016
Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review.
Shen H et al.
Bmc Pediatrics, 2014
Recurrent exercise-induced acute renal failure in a young Pakistani man with severe renal hypouricemia and SLC2A9 compound heterozygosity.
Jeannin G et al.
Bmc Medical Genetics, 2014
Acute kidney injury in two children caused by renal hypouricaemia type 2.
Stiburkova B et al.
Pediatric Nephrology (berlin, Germany), 2012
SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout.
Vitart V et al.
Nature Genetics, 2008
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