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Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese family

Developmental BiologyGenetic DisorderJapanese FamilyGeneticsGenetic EpidemiologyAudiologyLinkage AnalysisAuditory PhysiologyAuditory ResearchAuditory ScienceDfna6/14 MutationArtsMedicineHuman HearingAuditory SystemHearing Loss