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Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutation

Mendelian DisorderMitochondrial FunctionGenetic DisorderRrna C1494t MutationGeneticsAudiologyMolecular BiologyFour-generation Chinese FamilyMolecular GeneticsCochlear DevelopmentArtsMedicineMitochondrial 12SMolecular MedicineHearing Loss