LETTER TO THE EDITOR
Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families
Article first published online: 23 NOV 2012
© 2012 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd
Volume 84, Issue 3, pages 294–296, September 2013
How to Cite
Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families., , , , , , , , , .
- Issue published online: 12 AUG 2013
- Article first published online: 23 NOV 2012
- Higher Education Commission
- National Institutes of Health (NIH) – National Institute of Deafness and Communication Disorders. Grant Number: DC03594 and DC011651
- NIH. Grant Number: N01-HG-65403
|cge12047-sup-0001-TableS1.doc||Word document||68K||Table S1. LOD scores for families 4223, 4309 and 4526 within the 16p region which includes the OTOA*.|
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