Associated Papers
Literature review on congenital glucose-galactose malabsorption from 2001 to 2019.
Wang W et al.
Journal of Paediatrics and Child Health, 2020
Relevance of solute carrier family 5 transporter defects to inherited and acquired human disease.
Cannizzaro M et al.
Journal of Applied Genetics, 2019
Genetic Variants in SGLT1, Glucose Tolerance, and Cardiometabolic Risk.
Seidelmann SB et al.
Journal of the American College of Cardiology, 2018
Cross-comparison of the genome sequences from human, chimpanzee, Neanderthal and a Denisovan hominin identifies novel potentially compensated mutations.
Zhang G et al.
Human Genomics, 2011
Multiple sequence variations in SLC5A1 gene are associated with glucose-galactose malabsorption in a large cohort of Old Order Amish.
Xin B et al.
Clinical Genetics, 2011
Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption.
Martín MG et al.
Nature Genetics, 1996
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