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Details on Person Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia
| Class:Id | LiteratureReference:561250 |
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| _displayName | Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia |
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| _timestamp | 2010-03-31 12:29:49 |
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| author | [Person:561243] Wakida, N
[Person:561227] Tuyen, DG
[Person:166987] Adachi, M
[Person:503935] Miyoshi, T
[Person:561232] Nonoguchi, H
[Person:561228] Oka, T
[Person:561238] Ueda, O
[Person:561236] Tazawa, M
[Person:561244] Kurihara, S
[Person:561254] Yoneta, Y
[Person:111203] Shimada, H
[Person:444693] Oda, T
[Person:143389] Kikuchi, Y
[Person:75538] Matsuo, H
[Person:561036] Hosoyamada, M
[Person:352110] Endou, H
[Person:561234] Otagiri, M
[Person:561230] Tomita, K
[Person:419800] Kitamura, K |
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| created | [InstanceEdit:561229] Jassal, Bijay, 2010-03-31 |
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| journal | J Clin Endocrinol Metab |
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| pages | 2169-74 |
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| pubMedIdentifier | 15634722 |
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| title | Mutations in human urate transporter 1 gene in presecretory reabsorption defect type of familial renal hypouricemia |
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| volume | 90 |
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| year | 2005 |
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| (literatureReference) | [Reaction:561253] SLC22A12 exchanges extracellular urate for cytosolic LACT [Homo sapiens]
[Pathway:5619071] Defective SLC22A12 causes renal hypouricemia 1 (RHUC1) [Homo sapiens]
[FailedReaction:5625210] Defective SLC22A12 does not exchange extracellular urate for cytosolic LACT [Homo sapiens] |
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