Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia

Journal of Clinical Endocrinology and Metabolism

Volumn 90, Issue 4, 2005, Pages 2169-2174

  Wakida, Naoki ^a   Do, Gia Tuyen ^a   Adachi, Masataka ^a   Miyoshi, Taku ^a   Nonoguchi, Hiroshi ^a   Oka, Toshiaki ^b   Ueda, Osamu ^b   Tazawa, Masahiro ^c   Kurihara, Satoshi ^d   Yoneta, Yoshitaka ^e   Shimada, Hajime ^e   Oda, Takashi ^f   Kikuchi, Yuichi ^f   Matsuo, Hirotaka ^f   Hosoyamada, Makoto ^g   Endou, Hitoshi ^g   Otagiri, Masaki ^a   Tomita, Kimio ^a   Kitamura, Kenichiro ^a,h  

^a KUMAMOTO UNIVERSITY   (Japan)

^b Sapporo Tokushukai Hospital   (Japan)

^c FUJITA HEALTH UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^d Kasukabe Shuwa Hospital   (Japan)

^e KITASATO UNIVERSITY MEDICAL CENTER   (Japan)

^f NATIONAL DEFENSE MEDICAL COLLEGE   (Japan)

^g KYORIN UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^h KUMAMOTO UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

URATE;

ARTICLE; CLINICAL ARTICLE; FAMILIAL DISEASE; GENE; GENE EXPRESSION; GENE IDENTIFICATION; GENE MUTATION; GENE SEGREGATION; GENE SEQUENCE; GENETIC CODE; HUMAN; HUMAN URATE TRANSPORTER 1 GENE; HYPOURICEMIA; MUTATIONAL ANALYSIS; OOCYTE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; WILD TYPE; XENOPUS;

ADOLESCENT; ADULT; AGED; CARRIER PROTEINS; CHILD; FEMALE; GENOTYPE; HUMANS; MALE; MICROSATELLITE REPEATS; MIDDLE AGED; MUTATION; ORGANIC ANION TRANSPORTERS; ORGANIC CATION TRANSPORT PROTEINS; RENAL TUBULAR TRANSPORT, INBORN ERRORS; URIC ACID;

EID: 20244387960     PISSN: 0021972X     EISSN: None     Source Type: Journal    
DOI: 10.1210/jc.2004-1111     Document Type: Article

References (18)

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