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Mutation analyses by next-generation sequencing and multiplex ligation-dependent probe amplification in Japanese autosomal dominant polycystic kidney disease patients

Mendelian DisorderMedicineGeneticsRenal PathologyChronic Kidney DiseaseNext-generation SequencingPathologyDisease Gene IdentificationMutation AnalysesMolecular DiagnosticsNephrologyKidney ResearchClinical Genetics