Association between SLC2A9 transporter gene variants and uric acid phenotypes in African American and white families

Rheumatology

Volumn 50, Issue 5, 2011, Pages 871-878

  Rule, Andrew D ^a   de Andrade, Mariza ^a   Matsumoto, Martha ^a   Mosley, Tom H ^b   Kardia, Sharon ^c   Turner, Stephen T ^a  

^a MAYO CLINIC   (United States)

^b UNIVERSITY OF MISSISSIPPI MEDICAL CENTER   (United States)

^c UNIVERSITY OF MICHIGAN   (United States)

Author keywords

Fractional excretion of urate; Genetic epidemiology; Race; SLC2A9; Uric acid

Indexed keywords

CREATININE; URIC ACID;

ADULT; AFRICAN AMERICAN; ARTICLE; EUROPEAN AMERICAN; FEMALE; GENE; GENE LOCUS; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; KIDNEY CLEARANCE; KIDNEY TUBULE ABSORPTION; MAJOR CLINICAL STUDY; MALE; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SLC2A9 GENE; URIC ACID BLOOD LEVEL;

AFRICAN AMERICANS; AGED; BIOLOGICAL TRANSPORT; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; GENOTYPE; GLUCOSE TRANSPORT PROTEINS, FACILITATIVE; HUMANS; HYPERURICEMIA; KIDNEY; MALE; MIDDLE AGED; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; URIC ACID;

EID: 79955148941     PISSN: 14620324     EISSN: 14620332     Source Type: Journal    
DOI: 10.1093/rheumatology/keq425     Document Type: Article

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