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References

These sources were used to develop the Genetics Home Reference gene summary on the SLC5A1 gene.

Brown GK. Glucose transporters: structure, function and consequences of deficiency. J Inherit Metab Dis. 2000 May;23(3):237-46. Review. PubMed citation
Entrez Gene
Lam JT, Martín MG, Turk E, Hirayama BA, Bosshard NU, Steinmann B, Wright EM. Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects. Biochim Biophys Acta. 1999 Feb 24;1453(2):297-303. PubMed citation
OMIM: SOLUTE CARRIER FAMILY 5 (SODIUM/GLUCOSE COTRANSPORTER), MEMBER 1
Wright EM, Hirayama BA, Loo DF. Active sugar transport in health and disease. J Intern Med. 2007 Jan;261(1):32-43. Review. PubMed citation
Wright EM, Martín MG, Turk E. Intestinal absorption in health and disease--sugars. Best Pract Res Clin Gastroenterol. 2003 Dec;17(6):943-56. Review. PubMed citation
Wright EM, Turk E, Martin MG. Molecular basis for glucose-galactose malabsorption. Cell Biochem Biophys. 2002;36(2-3):115-21. Review. PubMed citation
Wright EM, Turk E. The sodium/glucose cotransport family SLC5. Pflugers Arch. 2004 Feb;447(5):510-8. Epub 2003 May 14. Review. Erratum in: Pflugers Arch. 2004 Feb;447(5):813-5. PubMed citation
Wright EM. I. Glucose galactose malabsorption. Am J Physiol. 1998 Nov;275(5 Pt 1):G879-82. Review. PubMed citation

Reviewed: July 2007

Published: May 20, 2013