Alterations in the GJB3 and CLDN14 genes in families with nonsyndromic sensorineural hearing loss

Genet Couns. 2005;16(3):309-11.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Claudins
  • Connexins / genetics*
  • Female
  • Gene Deletion
  • Genotype
  • Hearing Loss, Sensorineural / diagnosis
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Pedigree
  • Point Mutation / genetics
  • Polymerase Chain Reaction

Substances

  • Claudins
  • Connexins
  • Membrane Proteins
  • GJB3 protein, human
  • claudin 14