Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation

This publication has 24 references indexed in Scilit:

• Molecular Pathogenetic Mechanism of Maternally Inherited Deafness
  Annals of the New York Academy of Sciences, 2004
• 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
  American Journal of Human Genetics, 2004
• Cosegregation of C‐insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing loss
  American Journal of Medical Genetics Part A, 2003
• Inherited susceptibility to aminoglycoside ototoxicity: Genetic heterogeneity and clinical implications
  American Journal of Otolaryngology, 1999
• Mitochondrial deafness mutations reviewed
  Human Mutation, 1999
• Familial Progressive Sensorineural Deafness Is Mainly Due to the mtDNA A1555G Mutation and Is Enhanced by Treatment with Aminoglycosides
  American Journal of Human Genetics, 1998
• Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.
  Journal of Medical Genetics, 1997
• Non-Syndromic Deafness Associated with a Mutation and a Polymorphism in the Mitochondrial 12S Ribosomal RNA Gene in a Large Zairean Pedigree
  European Journal of Human Genetics, 1996
• Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness
  Pharmacogenetics, 1995
• Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness
  Nature Genetics, 1993