Author:
Lee HyunKyung,Han Kyoung Hee,Park Hye Won,Shin Jae Il,Kim Chan Jong,Namgung Mee Kyung,Kim Kee Hyuck,Koo Ja Wook,Chung Woo Young,Lee Dae-Yeol,Kim Su-Yung,Cheong Hae Il
Publisher
Springer Science and Business Media LLC
Subject
Nephrology,Pediatrics, Perinatology and Child Health
Reference18 articles.
1. Santer R, Kinner M, Schneppenheim M, Hillebrand G, Kemper M, Ehrich J, Swift P, Skovby F, Schaub J (2000) The molecular basis of renal glucosuria: mutations in the gene for a renal glucose transporter (SGLT2) [Abstract]. J Inherit Metab Dis 23(Suppl 1):178
2. van den Heuvel LP, Assink K, Willemsen M, Monnens L (2002) Autosomal recessive renal glucosuria attributable to a mutation in the sodium glucose cotransporter (SGLT2). Hum Genet 111:544–547
3. Santer R, Kinner M, Lassen CL, Schneppeheim R, Eggert P, Bald M, Brodehl J, Daschner M, Ehrich JHH, Kemper M, Volti SL, Neuhaus T, Skovby F, Swift PGF, Schaub J, Klaerke D (2003) Molecular analysis of the SGLT2 gene in patients with renal glucosuria. J Am Soc Nephrol 14:2873–2882
4. Francis J, Zhang J, Farhi A, Carey H, Geller DS (2004) A novel SGLT2 mutation in a patient with autosomal recessive renal glucosuria. Nephrol Dial Transplant 19:2893–2895
5. Kleta R, Stuart C, Gill FA, Gahl WA (2004) Renal glucosuria due to SGLT2 mutations. Mol Genet Metab 82:56–58
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