Defects in Na+/glucose cotransporter (SGLT1) trafficking and function cause glucose-galactose malabsorption

Nature Genetics

Volumn 12, Issue 2, 1996, Pages 216-220

  Martín, Martín G ^a   Turk, Eric ^a   Lostao, M Pilar ^a   Kerner, Cynthia ^a   Wright, Ernest M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; GALACTOSE; GLUCOSE; GLUCOSE TRANSPORTER; SODIUM ION;

ACTIVE TRANSPORT; ANIMAL CELL; ARTICLE; CLINICAL ARTICLE; GENETIC SCREENING; HUMAN; INFANTILE DIARRHEA; INTESTINE BRUSH BORDER; ION CURRENT; MALABSORPTION; MISSENSE MUTATION; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; XENOPUS;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; BIOLOGICAL TRANSPORT; CELL MEMBRANE; GALACTOSE; GLUCOSE; HETEROZYGOTE DETECTION; HOMOZYGOTE; HUMANS; MALABSORPTION SYNDROMES; MEMBRANE GLYCOPROTEINS; MEMBRANE POTENTIALS; METHYLGLUCOSIDES; MOLECULAR SEQUENCE DATA; MONOSACCHARIDE TRANSPORT PROTEINS; MUTATION; OOCYTES; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; PROTEIN STRUCTURE, SECONDARY; SODIUM-GLUCOSE TRANSPORTER 1; XENOPUS LAEVIS;

EID: 0030070055     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0296-216     Document Type: Article

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