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Details on Person Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria
| Class:Id | LiteratureReference:429604 |
|---|---|
| _displayName | Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria |
| _timestamp | 2009-07-17 12:31:36 |
| author | [Person:429639] Calado, J [Person:429658] Soto, K [Person:429611] Clemente, C [Person:429632] Correia, P [Person:429641] Rueff, J |
| created | [InstanceEdit:429634] Jassal, Bijay, 2009-07-17 |
| journal | Hum Genet |
| pages | 314-6 |
| pubMedIdentifier | 14614622 |
| title | Novel compound heterozygous mutations in SLC5A2 are responsible for autosomal recessive renal glucosuria |
| volume | 114 |
| year | 2004 |
| (literatureReference) | [Reaction:189208] SLC5A2 cotransports Na+ and glucose from extracellular region to cytosol [Homo sapiens] [Reaction:429613] SLC5As, NAGLT1 cotransport Glc and Na+ from extracellular region to cytosol [Homo sapiens] [FailedReaction:5658163] Defective SLC5A2 does not cotransport Glc and Na+ from extracellular region to cytosol [Homo sapiens] |
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