Ion channel defects in hereditary hearing loss

Neuron. 1999 Feb;22(2):217-9. doi: 10.1016/s0896-6273(00)81083-1.
No abstract available

Publication types

  • Review

MeSH terms

  • Animals
  • Connexin 26
  • Connexins / genetics
  • Hearing Disorders / genetics*
  • Humans
  • Ion Channels / genetics*
  • Mutation / genetics
  • Potassium Channels / genetics

Substances

  • Connexins
  • Ion Channels
  • Potassium Channels
  • Connexin 26
  • GJB3 protein, human