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5. URAT1 mutations cause renal hypouricemia type 1 in Iraqi Jews. Dinour D; Bahn A; Ganon L; Ron R; Geifman-Holtzman O; Knecht A; Gafter U; Rachamimov R; Sela BA; Burckhardt G; Holtzman EJ Nephrol Dial Transplant; 2011 Jul; 26(7):2175-81. PubMed ID: 21148271 [TBL] [Abstract][Full Text] [Related]
6. Homozygous frameshift mutation in the SLC22A12 gene in a patient with primary gout and high levels of serum uric acid. Vázquez-Mellado J; Alvarado-Romano V; Burgos-Vargas R; Jiménez-Vaca AL; Pozo-Molina G; Cuevas-Covarrubias SA J Clin Pathol; 2007 Aug; 60(8):947-8. PubMed ID: 17660342 [No Abstract] [Full Text] [Related]
7. High-resolution melting analysis for the rapid detection of an intronic single nucleotide polymorphism in SLC22A12 in male patients with primary gout in China. Guan M; Zhang J; Chen Y; Liu W; Kong N; Zou H Scand J Rheumatol; 2009; 38(4):276-81. PubMed ID: 19306160 [TBL] [Abstract][Full Text] [Related]
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11. New insights into renal transport of urate. Anzai N; Kanai Y; Endou H Curr Opin Rheumatol; 2007 Mar; 19(2):151-7. PubMed ID: 17278930 [TBL] [Abstract][Full Text] [Related]
12. A common mutation in an organic anion transporter gene, SLC22A12, is a suppressing factor for the development of gout. Taniguchi A; Urano W; Yamanaka M; Yamanaka H; Hosoyamada M; Endou H; Kamatani N Arthritis Rheum; 2005 Aug; 52(8):2576-7. PubMed ID: 16059895 [No Abstract] [Full Text] [Related]
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20. Functional analysis of novel allelic variants in URAT1 and GLUT9 causing renal hypouricemia type 1 and 2. Mancikova A; Krylov V; Hurba O; Sebesta I; Nakamura M; Ichida K; Stiburkova B Clin Exp Nephrol; 2016 Aug; 20(4):578-584. PubMed ID: 26500098 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]