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Defective SLC5A1 Causes Congenital Glucose/Galactose Malabsorption (GGM)

Instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5656364).

Statements about Defective SLC5A1 Causes Congenital Glucose/Galactose Malabsorption (GGM)

Part Of

SLC Transporter Disorders

Instance Of

Biological Pathway

Has Part(s)

Exact Match

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Defective SLC5A1 Does Not Cotransport Glc and Na+