Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss

Similar Items

• 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
  od: Zhao, Hui, i dr.
  Izdano: (2004)
• Mutational analysis of the mitochondrial 12S rRNA gene in Chinese pediatric subjects with aminoglycoside-induced and non-syndromic hearing loss
  od: Li, Zhiyuan, i dr.
  Izdano: (2005)
• Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss
  od: Lu, Jianxin, i dr.
  Izdano: (2010)
• Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees
  od: Chen, Jianfu, i dr.
  Izdano: (2007)
• Cosegregation of the G7444A Mutation in the Mitochondrial COI/tRNA(Ser(UCN)) Genes with the 12S rRNA A1555G Mutation in a Chinese Family with Aminoglycoside-induced and Nonsyndromic Hearing Loss
  od: Yuan, Huijun, i dr.
  Izdano: (2005)