A novel SGLT2 mutation in a patient with autosomal recessive renal glucosuria

Nephrology Dialysis Transplantation

Volumn 19, Issue 11, 2004, Pages 2893-2895

  Francis, Jean ^a   Zhang, Junhui ^a   Farhi, Anita ^a   Carey, Hugh ^a   Geller, David S ^a  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Glucosuria; SGLT2

Indexed keywords

BETA 2 MICROGLOBULIN; CARRIER PROTEINS AND BINDING PROTEINS; CREATININE; GLUCOSE; PHOSPHATE; SODIUM GLUCOSE COTRANSPORTER TYPE 2; UNCLASSIFIED DRUG;

ACIDOSIS; ADULT; AMINOACIDURIA; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; BETA 2 MICROGLOBULIN URINE LEVEL; CASE REPORT; CONSANGUINEOUS MARRIAGE; CREATININE CLEARANCE; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; FEMALE; GENE MUTATION; HUMAN; HYPERGLYCEMIA; HYPERTENSION; NUCLEIC ACID BASE SUBSTITUTION; PHOSPHATURIA; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROTEINURIA; PYELONEPHRITIS; RENAL DIABETES; SEQUENCE ANALYSIS;

AGED; AGED, 80 AND OVER; FEMALE; GLYCOSURIA, RENAL; HUMANS; MONOSACCHARIDE TRANSPORT PROTEINS; MUTATION; SODIUM-GLUCOSE TRANSPORTER 2;

EID: 8344257283     PISSN: 09310509     EISSN: None     Source Type: Journal    
DOI: 10.1093/ndt/gfh426     Document Type: Article

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