Phenotypic and Functional Analysis of Human SLC26A6 Variants in Patients With Familial Hyperoxaluria and Calcium Oxalate Nephrolithiasis

American Journal of Kidney Diseases

Volumn 52, Issue 6, 2008, Pages 1096-1103

  Monico, Carla G ^a   Weinstein, Adam ^b   Jiang, Zhirong ^b   Rohlinger, Audrey L ^a   Cogal, Andrea G ^a   Bjornson, Beth B ^a   Olson, Julie B ^a   Bergstralh, Eric J ^a   Milliner, Dawn S ^a   Aronson, Peter S ^b  

^a MAYO CLINIC   (United States)

^b YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

calcium oxalate urolithiasis; hyperoxaluria; SLC26A6

Indexed keywords

CALCIUM OXALATE; CARRIER PROTEIN; SLC26A6 PROTEIN; UNCLASSIFIED DRUG;

ADULT; AMINO ACID TRANSPORT; ANIMAL CELL; ARTICLE; CONTROLLED STUDY; FAMILIAL DISEASE; FEMALE; GENE MUTATION; GENETIC VARIABILITY; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HYPEROXALURIA; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; NEPHROLITHIASIS; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PROTEIN EXPRESSION; RISK FACTOR; URINE LEVEL; UROLITHIASIS; XENOPUS LAEVIS;

ADOLESCENT; ADULT; CALCIUM OXALATE; CASE-CONTROL STUDIES; CHILD, PRESCHOOL; CROSS-SECTIONAL STUDIES; FEMALE; HUMANS; HYPERCALCIURIA; MALE; MEMBRANE TRANSPORT PROTEINS; MIDDLE AGED; MUTATION; NEPHROLITHIASIS; PEDIGREE; PHENOTYPE; YOUNG ADULT;

EID: 56049089361     PISSN: 02726386     EISSN: None     Source Type: Journal    
DOI: 10.1053/j.ajkd.2008.07.041     Document Type: Article

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