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Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese Family

Mendelian DisorderMitochondrial FunctionGenetic DisorderGeneticsInherited Metabolic DiseaseLarge Chinese FamilyMolecular BiologyMolecular GeneticsNovel C1494t MutationDisease Gene IdentificationCochlear DevelopmentMedicineRrna Gene