The Molecular Basis of Glucose Galactose Malabsorption in a Large Swedish Pedigree
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Glucose-galactose malabsorption (GGM) is due to mutations in the gene coding for the intestinal sodium glucose cotransporter SGLT1 (SLC5A1). Here we identify the rare variant Gln457Arg (Q457R) in a large pedigree of patients in the Västerbotten County in Nort... ...
