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Autosomal recessive and sporadic deafness in Morocco: High frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant

Mendelian DisorderGenetic DisorderGeneticsAudiologySporadic DeafnessGjb2 MutationMolecular GeneticsDisease Gene IdentificationCochlear DevelopmentHigh FrequencyArtsMedicineHearing Loss