Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting

Kidney International

Volumn 69, Issue 5, 2006, Pages 852-855

  Calado, J ^a,e   Loeffler, J ^b   Sakallioglu, O ^c   Gok, F ^c   Lhotta, K ^b   Barata, J ^d   Rueff, J ^a  

^a UNIVERSIDADE NOVA DE LISBOA   (Portugal)

^b INNSBRUCK MEDICAL UNIVERSITY   (Austria)

^c GULHANE SCHOOL OF MEDICINE   (Turkey)

^d HOSPITAL DE SANTA CRUZ   (Portugal)

^e NOVA MEDICAL SCHOOL   (Portugal)

Author keywords

Glucosuria; Mutation; Renal; SGLT2; SLC5A2

Indexed keywords

ALDOSTERONE; RENIN;

ALDOSTERONE BLOOD LEVEL; ALLELISM; ARTICLE; CLINICAL ARTICLE; CODOMINANCE; CONTROLLED STUDY; FAMILIAL DISEASE; FRAMESHIFT MUTATION; GENE; GENE AMPLIFICATION; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC CODE; GENETIC SUSCEPTIBILITY; GLUCOSURIA; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; MOLECULAR DYNAMICS; MUTAGENESIS; MUTATIONAL ANALYSIS; NATRIURESIS; PEDIGREE ANALYSIS; PHENOTYPE; PLASMA RENIN ACTIVITY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RENAL DIABETES; RENIN ANGIOTENSIN ALDOSTERONE SYSTEM; SALT LOSING NEPHRITIS; SLC5A2 GENE;

DNA MUTATIONAL ANALYSIS; FEMALE; GLYCOSURIA, RENAL; HUMANS; MALE; MUTATION; PEDIGREE; PHENOTYPE; SODIUM CHLORIDE; SODIUM-GLUCOSE TRANSPORTER 2;

EID: 33644546432     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ki.5000194     Document Type: Article

References (18)

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