A Major Gene Affecting Age-Related Hearing Loss Is Common to at Least Ten Inbred Strains of Mice

This publication has 38 references indexed in Scilit:

• A Pro51Ser mutation in the COCH gene is associated with late onset autosomal dominant progressive sensorineural hearing loss with vestibular defects
  Human Molecular Genetics, 1999
• Functional Identification of the Mouse Circadian Clock Gene by Transgenic BAC Rescue
  Cell, 1997
• A high-resolution genetic map around waltzer on mouse Chromosome 10 and identification of a new allele of waltzer
  Mammalian Genome, 1997
• Mapping of DFNB12, a gene for a non-syndromal autosomal recessive deafness, to chromosome 10q21-22
  Human Molecular Genetics, 1996
• Role of transcription factors a Brn-3.1 and Brn-3.2 in auditory and visual system development
  Nature, 1996
• Genetics of age-related hearing loss in mice. III. Susceptibility of inbred and F1 hybrid strains to noise-induced hearing loss
  Hearing Research, 1996
• A comprehensive genetic map of the mouse genome
  Nature, 1996
• Genetic deafness--progress with mouse models
  Human Molecular Genetics, 1994
• Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains
  Hearing Research, 1993
• The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse
  Proceedings of the Royal Society of London. B. Biological Sciences, 1956