Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM) (Q45314797)

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An instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5656364)
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Defective SLC5A1 causes congenital glucose/galactose malabsorption (GGM)
An instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5656364)

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