Maternally inherited aminoglycoside-induced and nonsyndromic hearing loss is associated with the 12S rRNA C1494T mutation in three Han Chinese pedigrees

Lignende værker

• Mitochondrial 12S rRNA variants in 1642 Han Chinese pediatric subjects with aminoglycoside-induced and nonsyndromic hearing loss
  af: Lu, Jianxin, et al.
  Udgivet: (2010)
• 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
  af: Zhao, Hui, et al.
  Udgivet: (2004)
• Aminoglycoside Stress Together with the 12S rRNA 1494C>T Mutation Leads to Mitophagy
  af: Yu, Jialing, et al.
  Udgivet: (2014)
• The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family
  af: Liao, Zhisu, et al.
  Udgivet: (2007)
• Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss
  af: Zhao, Hui, et al.
  Udgivet: (2005)