Mitochondrial Mutations and Hearing Loss: Paradigm for Mitochondrial Genetics

This publication has 27 references indexed in Scilit:

• 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
• Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome
  The Journal of Pediatrics, 1993
• Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabetics
  The Lancet, 1993
• Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness
  Nature Genetics, 1993
• Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA
  The Lancet, 1992
• Tissue-specific expression and chromosome assignment of genes specifying two isoforms of subunit VIIa of human cytochrome c oxidase
  Gene, 1992
• Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
  Nature Genetics, 1992
• Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion
  Nature Genetics, 1992
• H-2M3 encodes the MHC Class I molecule presenting the maternally transmitted antigen of the mouse
  Cell, 1991
• Genetic aspects of antibiotic induced deafness: mitochondrial inheritance.
  Journal of Medical Genetics, 1991