Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish
- 9 December 2010
- journal article
- Published by Wiley in Clinical Genetics
- Vol. 79 (1), 86-91
- https://doi.org/10.1111/j.1399-0004.2010.01440.x
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- A Novel Mutation of Na+/Glucose Cotransporter in a Turkish Newborn with Congenital Glucose‐Galactose MalabsorptionJournal of Pediatric Gastroenterology and Nutrition, 2005
- The sodium/glucose cotransport family SLC5Pflügers Archiv - European Journal of Physiology, 2004
- Molecular Basis for Glucose-Galactose MalabsorptionCell Biochemistry and Biophysics, 2002
- A missense mutation in the Na+/glucose cotransporter gene SGLT1 in a patient with congenital glucose-galactose malabsorption: normal trafficking but inactivation of the mutant proteinBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 2001
- Missense mutations in SGLT1 cause glucose–galactose malabsorption by trafficking defectsBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1999
- Membrane Topology Motifs in the SGLT Cotransporter FamilyThe Journal of Membrane Biology, 1997
- Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorptionNature Genetics, 1996
- Membrane Topology of the Human Na+/Glucose Cotransporter SGLT1Online Journal of Public Health Informatics, 1996
- Congenital Selective Malabsorption of Glucose and GalactoseJournal of Pediatric Gastroenterology and Nutrition, 1985
- Chronic Diarrhoea Caused by Monosaccharide MalabsorptionActa Paediatrica, 1962