Diagnostic tests for primary renal hypouricemia

Nucleosides, Nucleotides and Nucleic Acids

Volumn 30, Issue 12, 2011, Pages 1112-1116

  Sebesta, Ivan ^a,b   Stiburkova, Blanka ^a   Bartl, Josef ^a   Ichida, Kimiyoshi ^c   Hosoyamada, Makoto ^d   Taylor, Judy ^e   Marinaki, Anthony ^e  

^a Charles University in Prague and General University Hospital in Prague   (Czech Republic)

^b CHARLES UNIVERSITY   (Czech Republic)

^c TOKYO UNIVERSITY OF PHARMACY AND LIFE SCIENCES   (Japan)

^d KEIO UNIVERSITY   (Japan)

^e ST THOMAS HOSPITAL   (United Kingdom)

Author keywords

Diagnostic tests; Renal hypouricemia; SLC22A12; SLC2A9; Uric acid transporter

Indexed keywords

URATE;

ACUTE KIDNEY FAILURE; ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL PROTOCOL; CZECH REPUBLIC; DIAGNOSTIC TEST; FEMALE; GENE; GENE DELETION; GENE INSERTION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC VARIABILITY; HUMAN; HURAT1 GENE; HYPERURICOSURIA; HYPOURICEMIA; MALE; NEPHROLITHIASIS; PRESCHOOL CHILD; PRIMARY RENAL HYPOURICEMIA; SLC22A12 GENE; SLC2A9 GENE; UNITED KINGDOM; URATV1 GENE; URIC ACID BLOOD LEVEL; URIC ACID URINE LEVEL; URINARY EXCRETION;

ADOLESCENT; ADULT; AGED; DIAGNOSTIC TECHNIQUES AND PROCEDURES; GLUCOSE TRANSPORT PROTEINS, FACILITATIVE; HUMANS; MIDDLE AGED; MUTATION; ORGANIC ANION TRANSPORTERS; ORGANIC CATION TRANSPORT PROTEINS; RENAL TUBULAR TRANSPORT, INBORN ERRORS; URINARY CALCULI; YOUNG ADULT;

EID: 84855892828     PISSN: 15257770     EISSN: 15322335     Source Type: Journal    
DOI: 10.1080/15257770.2011.611483     Document Type: Article

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