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Update of the spectrum of GJB2 gene mutations in 152 Moroccan families with autosomal recessive nonsyndromic hearing loss

Developmental BiologyMendelian DisorderGenetic DisorderGeneticsAudiologyGjb2 Gene MutationsMolecular GeneticsDisease Gene IdentificationCochlear DevelopmentMoroccan FamiliesArtsMedicineVariant InterpretationHearing Loss