How to Cite this Article: Fattahi Z, Shearer AE, Babanejad M, Bazazzadegan N, Almadani SN, Nikzat N, Jalalvand K, Arzhangi S, Esteghamat F, Abtahi R, Azadeh B, Smith RJH, Kahrizi K, Najmabadi H. 2012. Screening for MYO15A gene mutations in an autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population. Am J Med Genet Part A. 158A:1857–1864.
Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population†
Version of Record online: 26 JUN 2012
Copyright © 2012 Wiley Periodicals, Inc.
American Journal of Medical Genetics Part A
Volume 158A, Issue 8, pages 1857–1864, August 2012
How to Cite
Fattahi, Z., Shearer, A. E., Babanejad, M., Bazazzadegan, N., Almadani, S. N., Nikzat, N., Jalalvand, K., Arzhangi, S., Esteghamat, F., Abtahi, R., Azadeh, B., Smith, R. J.H., Kahrizi, K. and Najmabadi, H. (2012), Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population. Am. J. Med. Genet., 158A: 1857–1864. doi: 10.1002/ajmg.a.34411
- Issue online: 19 JUL 2012
- Version of Record online: 26 JUN 2012
- Manuscript Accepted: 1 NOV 2011
- Manuscript Received: 21 MAY 2011
- Iranian National Science Foundation. Grant Number: 85073/23
Additional supporting information may be found in the online version of this article.
|ajmg_34411_sm_SuppTab1.pdf||117K||Table I: Primers used for sequencing of Myo15A gene.|
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