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Compound Heterozygous Mutation of Na+/Glucose Cotransporter (SGLT1) Gene in a Japanese Patient with Congenital Glucose-Galactose Malabsorption (GGM). (October 2000)
Record Type:
Journal Article
Title:
Compound Heterozygous Mutation of Na+/Glucose Cotransporter (SGLT1) Gene in a Japanese Patient with Congenital Glucose-Galactose Malabsorption (GGM). (October 2000)
Main Title:
Compound Heterozygous Mutation of Na+/Glucose Cotransporter (SGLT1) Gene in a Japanese Patient with Congenital Glucose-Galactose Malabsorption (GGM)