Mutational analysis of idiopathic renal hypouricemia in Korea

Pediatric Nephrology

Volumn 20, Issue 7, 2005, Pages 886-890

  Cheong, Hae Il ^a   Kang, Ju Hyung ^a   Lee, Joo Hoon ^a   Ha, Il Soo ^a   Kim, Suhnggwon ^b   Komoda, Fusako ^c   Sekine, Takashi ^c   Igarashi, Takashi ^c   Choi, Yong ^a  

^a Seoul National University Children's Hospital   (South Korea)

^b Seoul National University Hospital   (South Korea)

^c UNIVERSITY OF TOKYO   (Japan)

Author keywords

Exercise induced acute renal failure; Hematuria; Renal hypouricemia; SLC22A12 gene; Urolithiasis

Indexed keywords

CREATININE; GENE PRODUCT; PROTEIN SLC22A12; UNCLASSIFIED DRUG; URIC ACID;

ACUTE KIDNEY FAILURE; ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; COMPUTER ASSISTED TOMOGRAPHY; CREATININE BLOOD LEVEL; FEMALE; GENE MUTATION; HEMATURIA; HETEROZYGOTE DETECTION; HUMAN; HYPOURICEMIA; IDIOPATHIC DISEASE; JAPAN; KOREA; MALE; MUTATIONAL ANALYSIS; PRIORITY JOURNAL; RETROSPECTIVE STUDY; URINALYSIS; UROLITHIASIS;

ADOLESCENT; ADULT; ARGININE; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; CARRIER PROTEINS; CHILD; DNA MUTATIONAL ANALYSIS; EXERCISE; FEMALE; HEMATURIA; HISTIDINE; HUMANS; KIDNEY DISEASES; KIDNEY FAILURE, ACUTE; MALE; MOLECULAR SEQUENCE DATA; MUTATION; ORGANIC ANION TRANSPORTERS; ORGANIC CATION TRANSPORT PROTEINS; TOMOGRAPHY, X-RAY COMPUTED; TRYPTOPHAN; URIC ACID; URINARY CALCULI;

EID: 21344469277     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-005-1863-3     Document Type: Article

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