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Identification of Two Novel Mutations in the CLCN5 Gene in Japanese Patients With Familial Idiopathic Low Molecular Weight Proteinuria (Japanese Dent's Disease)

Mendelian DisorderGenetic DisorderMedicineGeneticsInherited Metabolic DiseaseGenetic EpidemiologyPathologyJapanese DentMolecular GeneticsDisease Gene IdentificationGenomicsMolecular DiagnosticsClcn5 GeneJapanese PatientsClinical Genetics