A mutation in mitochondrial 12S rRNA, A827G, in Argentinean family with hearing loss after aminoglycoside treatment
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference30 articles.
1. Molecular genetics of hearing loss;Petit;Annu. Rev. Genet.,2001
2. Maternally inherited hearing impairment;Van;Clin. Genet.,2000
3. Mitochondrial ribosomal RNA gene mutation in a patient with sporadic aminoglycoside ototoxicity;Fischel-Ghodsian;Am. J. Otolaryngol.,1993
4. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness;Prezant;Nat. Genet.,1993
5. A molecular basis for human hypersensitivity to aminoglycoside antibiotics;Hutchin;Nucleic Acids Res.,1993
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