Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM) (Homo sapiens)
defective slc5a1 causes congenital glucose/galactose malabsorption (ggm) (homo sapiens)
Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM) (Homo sapiens)
defective slc5a1 causes congenital glucose/galactose malabsorption (ggm) (homo sapiens)