Article info

Download PDFPDF
Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss
  1. Correspondence to Dr Soo Y Yoong, St Luke's Hospital, Little Horton Lane, Bradford BD5 0NA, UK; soo.yoong{at}bradfordhospitals.nhs.uk
View Full Text

Citation

Yoong SY, Mavrogiannis LA, Wright J, et al
Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss

Publication history

  • Accepted April 8, 2011
  • First published May 17, 2011.
Online issue publication 
March 22, 2016

Article Versions

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.