A Case of Congenital Glucose Galactose Malabsorption with a New Mutation in the SLC5A1 Gene
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Congenital glucose-galactose malabsorption (CGGM) is an autosomal recessive disorder originating from an abnormal transporter mechanism in the intestines. It was sourced from a mutation in the SLC5A1 gene, which encodes a sodium-dependent glucose transporter. ... ...
