Genetic Conditions > glucose-galactose malabsorption >

References

These sources were used to develop the Genetics Home Reference condition summary on glucose-galactose malabsorption.

Brown GK. Glucose transporters: structure, function and consequences of deficiency. J Inherit Metab Dis. 2000 May;23(3):237-46. Review. PubMed citation
El-Naggar W, Balfe JW, Barbar M, Taha D. Nephrocalcinosis in glucose-galactose malabsorption, association with renal tubular acidosis. Pediatr Nephrol. 2005 Sep;20(9):1336-9. Epub 2005 Jul 12. PubMed citation
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: GLUCOSE/GALACTOSE MALABSORPTION
Scriver's Online Metabolic and Molecular Bases of Inherited Disease (OMMBID): Familial Glucose-Galactose Malabsorption and Hereditary Renal Glycosuria
Tasic V, Slaveska N, Blau N, Santer R. Nephrolithiasis in a child with glucose-galactose malabsorption. Pediatr Nephrol. 2004 Feb;19(2):244-6. Epub 2003 Dec 11. PubMed citation
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. I. Glucose galactose malabsorption. Am J Physiol. 1998 Nov;275(5 Pt 1):G879-82. Review. PubMed citation


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