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Molecular screening of deafness in Algeria: High genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F

Usher LociMolecular ScreeningGenetic DisorderGeneticsGenetic EpidemiologyHigh Genetic HeterogeneityGenetic FactorDisease Gene IdentificationCochlear DevelopmentMedicineGenetic BasisHearing Loss