Publication | Closed Access

Intrafamilial phenotype variability in patients with Gitelman syndrome having the same mutations in their thiazide-sensitive sodium/chloride cotransporter

Thiazide-sensitive Sodium/chloride CotransporterMendelian DisorderGenetic DisorderGeneticsPhysiologyInherited Metabolic DiseaseIntrafamilial Phenotype VariabilitySame MutationsMedicineVariant InterpretationClinical Genetics