Publication | Open Access

Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population

Gjb6 DeletionGenetic DisorderGeneticsAudiologyArtsGjb2 Gene MutationsAuditory PhysiologyMolecular GeneticsAuditory ResearchAuditory ScienceHuman HearingSouth African PopulationMedicineHearing Loss