References
- Prezant TR, Agapian JV, Bohlman MC, et al. Mito-chondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nature Genetics 1993; 4: 289–94.
- Hutchin T, Haworth I, Higashi K, et al. A molecular basis for human hypersensitivity to aminoglycoside an-tibiotics. Nucleic Acids Res 1993; 21: 4174–9.
- Fischel-Ghodsian N, Prezant TR, Bu X, Oztas S. Mito-chondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity. Am J Oto-laryngol 1993; 14: 399–403.
- Matthijs G, Claes S, Longo-Mbenza B, Cassiman J-J. Non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S riboso-mal RNA gene in a large Zairean pedigree. Eur J Hum Genet 1996; 4: 46–51.
- Tamagawa Y, Kitamura K, Ishida T, Hagiwara H, Abe K, Nishizawa M. Mitochondrial DNA mutation at nucleotide 1555 in a patient with bilateral sen-sorineural hearing loss of unknown etiology. Acta Oto-laryngol (Stockh) 1996; 116: 796–8.
- Chang SO, Oh CS, Kim HI, Chi Y. A maternally inherited mitochondrial rRNA mutation associated with aminoglycoside-induced deafness: a pedigree from Korea. Proceedings of the Association for Research in Otolaryngology Symposium, 1997; Abstract 876.
- El-Schahawi M, Lopez de Munain A, Sarrazin AM, et al. Two large Spanish pedigrees with nonsyndromic sensorineural deafness and the mtDNA mutation at nt 1555 in the 12S rRNA gene: evidence of heteroplasmy. Neurology 1997; 48: 453–6.
- Fischel-Ghodsian N, Prezant TR, Chaltraw WE, et al. Mitochondrial gene mutation is a significant predispos-ing factor in aminoglycoside ototoxicity. Am J Otolar-yngol 1997; 18: 173–8.
- Pandya A, Xia X, Radnaabazar J, et al. Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity. J Med Genet 1997; 34: 169–72.
- Usami S, Abe S, Kasai M, et al. Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation. Laryngoscope 1997; 107: 483–90.
- Gardner J, Goliath R, Viljoen D, et al. Streptomycin ototoxicity in a South African family: a mitochondrial disorder. J Med Genet. 1997; 34: 904–6.
- Estivill X, Govea N, Barcelo E, et al. Familial progres-sive sensorineural deafness is mainly due to the mtDNA A1555G mutation and is enhanced by treat-ment of aminoglycosides. Am J Hum Genet 1998; 62: 27–35.
- Yuan H, Jiang S, Yang W, et al. Mutation analysis of mitochondrial 12S and 16S ribosomal RNA genes for pedigrees with aminoglycoside antiobiotic induced deafness: a novel discovery. Proceedings of the Associ-ation for Research in Otolaryngology Symposium, 1998; Abstract 185.
- Hu D-N, Qiu W-Q, Wu B-T, et al. Genetic aspects of antibiotic induced deafness: mitochondrial inheritance. J Med Genet 1991; 28: 79–83.
- Higashi K. Unique inheritance of streptomycin-induced deafness. Clin Genet 1989; 35: 433–6.
- Viljoen DL, Sellars SL, Beighton P. Familial aggrega-tion of streptomycin ototoxicity: autosomal dominant inheritance? J Med Genet 1983; 20: 357–60.
- Braverman I, Jaber L, Levi H, et al. Audiovestibular findings in patients with deafness caused by a mito-chondrial susceptibility mutation and precipitated by an inherited mutation or aminoglycosides. Arch Oto-laryngol Head Neck Surg 1996; 122: 1001–4.
- Hutchin TP, Cortopassi GA. Multiple origins of a mitochondrial mutation conferring deafness. Genetics 1997; 145: 771–6.
- Jaber L, Shohat M, Bu X, et al. Sensorineural deafness inherited as a tissue specific mitochondrial disorder. J Med Genet 1992; 29: 86–90.
- Gold M, Rapin I. Non-Mendelian mitochondrial inher-itance as a cause of progressive genetic sensorineural hearing loss. Int J Pediatr Otorhinolaryngol 1994; 30: 91–104.
- Moazed D, NoIler HF. Interaction of antibiotics with functional sites in 16S ribosomal RNA. Nature 1987; 327: 389–94.
- De Stasio EA, Moazed D, NoIler HF, Dahlberg AE. Mutations in 16S ribosomal RNA disrupt antibiotic-RNA interactions. EMBO J 1989; 8: 1213–6.
- Inoue K, Takai D, Soejima A, et al. Mutant mtDNA at 1555 A to G in 12S rRNA gene and hypersuscepti-bility of mitochondrial translation to streptomycin can be co-transferred to p HeLa cells. Biochem Biophys Res Commun 1996; 223: 496–501.
- Guan M-X, Fischel-Ghodsian N, Attardi G. Biochemi-cal evidence for nuclear gene involvement in phenotype of non-syndromic deafness associated with mitochon-drial 12S rRNA mutation. Hum Mol Genet 1996; 5: 963 —71.
- Lindsay JR, Hinojosa R. Histopathologic features of the inner ear associated with Kearns—Sayre syndrome. Arch Otolaryngol 1976; 102: 747–52.