Introduction The C allele of the nonsynonymous Arg265His (rs3733591) variant of SLC2A9
confers risk for gout in Han Chinese, Solomon Island and Japanese samples, with a …

Objective To study the associations of gout, tophi and uric acid levels with the gout-related
SLC2A9 (solute carrier family 2, member 9) single nucleotide polymorphisms (SNPs) …

Objective The aim of this study was to determine whether polymorphisms in solute carrier
family 2 and facilitated glucose transporter member 9 (SLC2A9) are associated with …

Background Gout is a highly hereditary disease, but not all those carrying well-known risk
variants have developing gout attack even in hyperuricemia status. We performed a genome …

Gout is characterised by monosodium urate crystals in hyperuricaemic individuals. 1 2
Impaired excretion of urate exacerbates this condition. 1 Urate transporter 1 (encoded by …

Introduction There is inconsistent association between urate transporters SLC22A11
(organic anion transporter 4 (OAT4)) and SLC22A12 (urate transporter 1 (URAT1)) and risk …

Aim The main objective of this study is to elucidate the clinical significance of the SLC
2A9/GLUT 9 rs11722228 polymorphism among male gout patients. Method We …

Objective To examine the role of genetic variation in the renal urate transporter SLC2A9 in
gout in New Zealand sample sets of Māori, Pacific Island, and Caucasian ancestry and to …

The relationship between the SLC2A9 (solute carrier family 2, member 9) gene
polymorphisms and gout was still inconsistent among the individual genetic association …

Introduction Two major gout-causing genes have been identified, the urate transport genes
SLC2A9 and ABCG2. Variation within the SLC17A1 locus, which encodes sodium …