Majid Fardaee

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Fanconi–Bickel syndrome (FBS: MIM227810) or glycogen storage disease type XI (GSD11) is a rare autosomal recessive disorder caused by defects in the facilitative glucose transporter 2 (GLUT2), which transports glucose in and out of the hepatocytes, pancreatic β cells, and the basolateral membranes of the interstitial and renal epithelial cells. The affected(More)
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