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Zahedan Journal of Research in Medical Sciences
The Official Journal of Zahedan University of Medical Sciences
Outlines
The contribution of autosomaul recessive non-syndromic deafness to DFNB59 mutations (Pejvakin)
Author(s):
Marzieh Abolhasani1, Effat Farrokhi2, Mohsen Noorbakhsh3, Maryam Taherzadeh2, Fatemeh Azadegan1, Azam Asgari4, Morteza Hashmzadeh5,*1BSc of Genetic, Cellular and Molecular Research Center, Shahrekord University of Medical Sciences and Health Services, Shahrekord, Iran.
2MSc of Biochemistery, Cellular and Molecular Reserch Center, Shahrekord University of Medical Sciences and Health Services, Shahrekord, Iran.
3Medical Student, Shahrekord University of Medical Sciences and Health Services, Shahrekord, Iran.
4MSc of Animal Physiology, Plant Reserch Center, Shahrekord University of Medical Sciences and Health Services, Shahrekord, Iran
5Professor of Human Genetics, Cellular and Molecular Reserch Center, Shahrekord University of Medical Sciences and Health Services, Shahrekord, Iran.
Published online:Aug 26, 2010
Article type:Research Article
Received:Feb 27, 2010
Accepted:Jul 17, 2010
How to Cite:Abolhasani M, Farrokhi E, Noorbakhsh M, Taherzadeh M, Azadegan F, et al. The contribution of autosomaul recessive non-syndromic deafness to DFNB59 mutations (Pejvakin). Zahedan J Res Med Sci. 2010;12(3):e94295. doi:
Abstract
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© 2010, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.
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