You are here

  • Home
  • Archive
  • Volume 37, Issue 11
  • Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE

Article info

Article menu
Download PDFPDF
Electronic letters
Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE

Authors

  1. Dr Ayadi, hammadi.ayadi@fmsf.rnu.tn
View Full Text

Citation

MASMOUDI S, ELGAIED-BOULILA A, KASSAB I, et al
Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE
Journal of Medical Genetics 2000;37:e39.

Publication history

  • First published November 1, 2000.
Online issue publication 
April 27, 2016

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Copyright information

Journal of Medical Genetics