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High homogeneity in auditory outcome of pediatric CI-patients with mutations in Gap-Junction-Protein Beta2

Pediatric OtolaryngologyGenetic DisorderPediatric AudiologyGeneticsAudiologyPediatricsPediatric Ci-patientsAuditory PhysiologyHigh HomogeneityAuditory ResearchAuditory ScienceHuman HearingArtsGap-junction-protein Beta2Hearing Loss