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Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation
- Correspondence to: Dr Paolo Gasparini Telethon Institute of Genetics and Medicine, Via P Castellino III, Torino I-71013, Italy; gasparini{at}tigem.it
Citation
Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation
Publication history
- Received February 15, 2005
- Accepted May 25, 2005
- Revised May 24, 2005
- First published June 1, 2005.
Online issue publication
April 27, 2016
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Copyright 2006 Journal of Medical Genetics