A major gene affecting age-related hearing loss in C57BL/6J mice

This publication has 32 references indexed in Scilit:

• mdfw:A Deafness Susceptibility Locus That Interacts with Deaf Waddler (dfw)
  Genomics, 1997
• The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
  Nature Genetics, 1995
• Defective myosin VIIA gene responsible for Usher syndrome type IB
  Nature, 1995
• Genes and deafness
  Trends in Genetics, 1994
• Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse
  Mammalian Genome, 1994
• A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene
  Human Molecular Genetics, 1994
• Genetic Epidemiology of Hearing Impairment
  Annals of the New York Academy of Sciences, 1991
• Morphology of the octopus cell area of the cochlear nucleus in young and aging C57BL/6J and CBA/J mice
  Journal of Comparative Neurology, 1990
• Development and degeneration of hearing in the c57/b16 mouse: Relation of electrophysiologic responses from the round window and cochlear nucleus to cochlear anatomy and behavioral responses
  The Laryngoscope, 1979
• Electron Microscopic Studies of Capillary Permeability in Normal and Ames Waltzer Deaf Mice
  Acta Oto-Laryngologica, 1971