At the speed of sound: gene discovery in the auditory system

B L Resendes, R E Williamson, C C Morton

Research output: Contribution to journalArticlepeer-review

Abstract

As auditory genes and deafness-associated mutations are discovered at a rapid rate, exciting opportunities have arisen to uncover the molecular mechanisms underlying hearing and hearing impairment. Single genes have been identified to be pathogenic for dominant or recessive forms of nonsyndromic hearing loss, syndromic hearing loss, and, in some cases, even multiple forms of hearing loss. Modifier loci and genes have been found, and investigations into their role in the hearing process will yield valuable insight into the fundamental processes of the auditory system.

Original languageEnglish
Pages (from-to)923-35
Number of pages13
JournalAmerican Journal of Human Genetics
Volume69
Issue number5
DOIs
Publication statusPublished - Nov 2001

Keywords

  • Deafness
  • Extracellular Matrix
  • Hearing
  • Homeostasis
  • Humans
  • Ions
  • Mutation
  • Phenotype
  • Transcription Factors
  • Journal Article
  • Review

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