HypercalciuriaCalcium Metabolism DisordersNephrocalcinosisSodium-Phosphate Cotransporter Proteins, Type IIcKidney CalculiNephrolithiasisPoint MutationMutation, MissenseFamilial Hypophosphatemic RicketsMutationRenal Tubular Transport, Inborn ErrorsUrinary CalculiClaudinsUrolithiasisCalciumPotassium CitratePedigreeFrameshift MutationCalcium OxalateHypercalcemiaGerm-Line MutationSodium-Phosphate Cotransporter Proteins, Type IReceptors, Calcium-SensingMagnesium DeficiencyHyperoxaluriaParathyroid HormoneHypophosphatemia, FamilialUrine Specimen CollectionHeterozygoteCalbindin 1PhosphorusChlorothiazideCalbindinsBase SequenceDNA Mutational AnalysisCalcitriolHypoparathyroidismTrichlormethiazide14-alpha Demethylase InhibitorsBartter SyndromeMutation RateOxalatesFanconi SyndromeHomozygotePhenotypeMolecular Sequence DataAcidosis, Renal TubularS100 Calcium Binding Protein GExonsDent DiseaseNocturnal EnuresisPhosphatesAmino Acid SubstitutionGenotypeGenes, DominantDihydrotachysterolMagnesiumCalcium, DietaryGenetic LinkageTRPV Cation ChannelsKidneyAntidiuretic AgentsPolymerase Chain ReactionSodium-Phosphate Cotransporter Proteins, Type IIIAmino Acid SequenceAllelesSyndromeThiazidesHypocalcemiaChromosome MappingPolymorphism, Single-Stranded ConformationalKidney TubulesChloride ChannelsMutagenesis, Site-DirectedCreatinineCitric AcidHyperparathyroidismCodon, NonsenseSodium Chloride Symporter InhibitorsMutagenesisFamily HealthUrinalysisUric AcidSequence Analysis, DNAHydrochlorothiazideVesico-Ureteral RefluxParathyroid DiseasesSodium-Phosphate Cotransporter ProteinsBone Diseases, MetabolicParathyroid GlandsGenes, RecessiveKidney Tubules, DistalMembrane ProteinsHematuriaGenetic Predisposition to DiseaseSequence DeletionGenetic TestingNephronsIntestinal AbsorptionProtein Structure, Tertiary