Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside-induced deafness
Bacino CM, Prezant TR, Bu X, et al. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside-induced deafness. Pharmacogenetics 1995; 5:165-72.
Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycoside
Estivill X, Govea N, Barcelo A, et al. Familial progressive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treatment with aminoglycoside. Am J Hum Genet 1998; 62:27-35.
Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity
Fischel-Ghodsian N, Prezant TR, Bu X, Oztas S. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity. Am J Otolaryngol 1993; 14:399-403.
Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A→G mitochondrial mutation
Abe S, Kelley PM, Kimberling WJ, et al. Connexin 26 gene (GJB2) mutation modulates the severity of hearing loss associated with the 1555A→G mitochondrial mutation. Am J