Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE

J Med Genet. 2000 Nov;37(11):E39. doi: 10.1136/jmg.37.11.e39.
No abstract available

Publication types

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

MeSH terms

  • Connexin 26
  • Connexins / genetics*
  • DNA Mutational Analysis
  • Electrophoresis, Polyacrylamide Gel / methods
  • Gene Frequency
  • Hearing Loss, Sensorineural / epidemiology
  • Hearing Loss, Sensorineural / genetics*
  • Heterozygote*
  • Humans
  • Prevalence
  • Tunisia / epidemiology

Substances

  • Connexins
  • GJB2 protein, human
  • Connexin 26