Associated Papers
Literature review on congenital glucose-galactose malabsorption from 2001 to 2019.
Wang W et al.
Journal of Paediatrics and Child Health, 2020
Nutrition management of congenital glucose-galactose malabsorption: Case report of a Chinese infant.
Ma M et al.
Medicine, 2019
Molecular analysis of the SGLT2 gene in patients with renal glucosuria.
Santer R et al.
Journal of the American Society of Nephrology : Jasn, 2003
Molecular basis for glucose-galactose malabsorption.
Wright EM et al.
Cell Biochemistry and Biophysics, 2002
Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption.
Martín MG et al.
Nature Genetics, 1996
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