These authors contributed equally to this work.
A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family†
Version of Record online: 12 FEB 2009
Copyright © 2009 Wiley-Liss, Inc.
American Journal of Medical Genetics Part A
Volume 149A, Issue 3, pages 555–558, March 2009
How to Cite
Shearer, A. E., Hildebrand, M. S., Bromhead, C. J., Kahrizi, K., Webster, J. A., Azadeh, B., Kimberling, W. J., Anousheh, A., Nazeri, A., Stephan, D., Najmabadi, H., Smith, R. J.H. and Bahlo, M. (2009), A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family. Am. J. Med. Genet., 149A: 555–558. doi: 10.1002/ajmg.a.32670
How to cite this article: Shearer AE, Hildebrand MS, Bromhead CJ, Kahrizi K, Webster JA, Azadeh B, Kimberling WJ, Anousheh A, Nazeri A, Stephan D, Najmabadi H, Smith RJH, Bahlo M. 2009. A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family. Am J Med Genet Part A 149A:555–558.
- Issue online: 24 FEB 2009
- Version of Record online: 12 FEB 2009
- Manuscript Accepted: 24 OCT 2008
- Manuscript Received: 15 AUG 2008
- National Institutes of Health (NIH)-National Institute on Deafness and Other Communication Disorders (NIDCD). Grant Number: R01 DC02842
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