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The prevalence of mitochondrial mutations associated with aminoglycoside-induced deafness in ethnic Latvian population: the appraisal of the evidence

Mendelian DisorderGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic EpidemiologyAudiologyMitochondrial MutationsAminoglycoside-induced DeafnessArtsMedicineEthnic Latvian PopulationHearing Loss