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Digenic inheritance in autosomal recessive non-syndromic hearing loss cases carrying GJB2 heterozygote mutations: Assessment of GJB4, GJA1, and GJC3

Developmental BiologyMendelian DisorderGjb2 Heterozygote MutationsGenetic DisorderGeneticsAudiologyMolecular GeneticsCochlear DevelopmentAuditory ScienceHuman HearingArtsMedicineDigenic InheritanceHearing Loss