Missense mutations in SGLT1 cause glucose-galactose malabsorption by trafficking defects

Biochimica et Biophysica Acta - Molecular Basis of Disease

Volumn 1453, Issue 2, 1999, Pages 297-303

  Lam, Jason T ^a   Martín, Martín G ^a   Turk, Eric ^a   Hirayama, Bruce A ^a   Bosshard, Nils U ^b   Steinmann, Beat ^b   Wright, Ernest M ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY CHILDREN S HOSPITAL   (Switzerland)

Author keywords

Glucose galactose malabsorption; Human Na+ glucose cotransporter 1 (hSGLT1); Protein trafficking

Indexed keywords

GALACTOSE; GLUCOSE; SODIUM GLUCOSE COTRANSPORTER; UNCLASSIFIED DRUG;

ARTICLE; CASE REPORT; DIARRHEA; FEMALE; GENE MUTATION; HUMAN; IMMUNOBLOTTING; MALABSORPTION; MISSENSE MUTATION; NEWBORN; OOCYTE; PRIORITY JOURNAL; SUGAR TRANSPORT;

CELL MEMBRANE; ENDOPLASMIC RETICULUM; FEMALE; GALACTOSE; GLUCOSE; HUMANS; INFANT, NEWBORN; MALABSORPTION SYNDROMES; MEMBRANE GLYCOPROTEINS; MONOSACCHARIDE TRANSPORT PROTEINS; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SODIUM-GLUCOSE TRANSPORTER 1;

XENOPUS LAEVIS;

EID: 0033032528     PISSN: 09254439     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0925-4439(98)00109-4     Document Type: Article

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