Article info
Electronic letters
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus
- Correspondence to: Dr Richard J H Smith Department of Otolaryngology and Head and Neck Surgery, Interdepartmental Genetics Program, The University of Iowa, 200 Hawkins Drive, Iowa City, IA 52242, USA; richard-smithuiowa.edu
Citation
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus
Publication history
- Received March 10, 2005
- Accepted July 4, 2005
- Revised June 30, 2005
- First published July 20, 2005.
Online issue publication
September 30, 2005
Article Versions
- Previous version (20 July 2005).
- You are viewing the most recent version of this article.
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
Copyright 2005 Journal of Medical Genetics