Clinical presentation of the DFNA loci where causative genes have not yet been cloned. DFNA4, DFNA6/14, DFNA7, DFNA16, DFNA20 and DFNA21

Adv Otorhinolaryngol. 2002:61:98-106. doi: 10.1159/000066820.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Auditory Threshold
  • Carrier Proteins / genetics*
  • Disease Progression
  • Genetic Linkage
  • Hearing Loss, Sensorineural / diagnosis
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Membrane Proteins / genetics*
  • Molecular Motor Proteins*
  • Mutation
  • Myosin Heavy Chains / genetics*
  • Myosin Type II
  • Phenotype*

Substances

  • Carrier Proteins
  • MYH14 protein, human
  • MYH9 protein, human
  • Membrane Proteins
  • Molecular Motor Proteins
  • wolframin protein
  • Myosin Type II
  • Myosin Heavy Chains