Human xanthine dehydrogenase cDNA sequence and protein in an atypical case of type I xanthinuria in comparison with normal subjects

Clinica Chimica Acta

Volumn 304, Issue 1-2, 2001, Pages 153-158

  Yamamoto, Tetsuya ^a   Moriwaki, Yuji ^a   Shibutani, Yuichi ^b   Matsui, Kiyoshi ^a   Ueo, Taro ^b   Takahashi, Sumio ^a   Tsutsumi, Zenta ^a   Hada, Toshikazu ^a  

^a HYOGO COLLEGE OF MEDICINE   (Japan)

^b NISHI KOBE MEDICAL CENTER   (Japan)

Author keywords

Hypouricemia; Oxypurines; Xanthine dehydrogenase cDNA; Xanthine oxidase deficiency; Xanthinuria

Indexed keywords

COMPLEMENTARY DNA; HYPOXANTHINE; MESSENGER RNA; OXIPURINOL; URIC ACID; XANTHINE DEHYDROGENASE; XANTHINE OXIDASE;

ARTICLE; CASE REPORT; CONTROLLED STUDY; DUODENUM MUCOSA; ENZYME ACTIVITY; ENZYME BLOOD LEVEL; HUMAN; HYPOURICEMIA; IMMUNOREACTIVITY; PRIORITY JOURNAL; PROTEIN SYNTHESIS; SEQUENCE ANALYSIS; URIC ACID BLOOD LEVEL; URINARY EXCRETION; XANTHINURIA;

BASE SEQUENCE; DNA PRIMERS; DNA, COMPLEMENTARY; HUMANS; POLYMERASE CHAIN REACTION; REFERENCE VALUES; RNA, MESSENGER; XANTHINE DEHYDROGENASE; XANTHINES;

EID: 0035146938     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0009-8981(00)00413-7     Document Type: Article

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6. Assignment of human xanthine dehydrogenase gene to chromosome 2P22
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8. Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria
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