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Details on Person Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter
| Class:Id | LiteratureReference:426108 |
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| _displayName | Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter |
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| _timestamp | 2009-06-12 13:18:19 |
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| author | [Person:426111] Simon, DB
[Person:426084] Nelson-Williams, C
[Person:426151] Bia, MJ
[Person:426115] Ellison, D
[Person:426113] Karet, FE
[Person:426129] Molina, AM
[Person:426135] Vaara, I
[Person:216583] Iwata, F
[Person:426092] Cushner, HM
[Person:426106] Koolen, M
[Person:426123] Gainza, FJ
[Person:426090] Gitleman, HJ
[Person:425672] Lifton, RP |
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| created | [InstanceEdit:426114] Jassal, Bijay, 2009-06-12 |
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| journal | Nat Genet |
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| pages | 24-30 |
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| pubMedIdentifier | 8528245 |
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| title | Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter |
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| volume | 12 |
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| year | 1996 |
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| (literatureReference) | [Reaction:426130] SLC12A3 cotransports Cl-, Na+ from extracellular region to cytosol [Homo sapiens]
[FailedReaction:5623705] Defective SLC12A3 does not cotransport Cl-, Na+ from extracellular region to cytosol [Homo sapiens] |
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