A new link between insulinoma and congenital glucose-galactose malabsorption
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Congenital glucose-galactose malabsorption (CGGM) is a rare autosomal recessive disorder caused by a biallelic mutation of solute carrier family 5 member 1 (SLC5A1), encoding the sodium-dependent glucose transport-1 (SGLT-1) protein. Patients with CGGM present... ...
