Spectrum of GJB2 mutations in Cypriot nonsyndromic hearing loss subjects

J Genet. 2014 Aug;93(2):471-6. doi: 10.1007/s12041-014-0365-0.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Connexin 26
  • Connexins / genetics*
  • Cyprus
  • DNA Mutational Analysis
  • Deafness / genetics
  • Gene Frequency
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Mutation, Missense
  • Sequence Deletion

Substances

  • Connexins
  • GJB2 protein, human
  • Connexin 26

Supplementary concepts

  • Nonsyndromic Deafness