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Genetics Research International
Volume 2017, Article ID 5836525, 3 pages
https://doi.org/10.1155/2017/5836525
Research Article

Frequency of c.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment

1Universitäts-HNO-Klinik Tübingen, Tübingen, Germany
2Department of Bioinformatics, Africa City of Technology, Khartoum, Sudan
3Faculty of Biotechnology, University of Malakand, Malakand, Pakistan
4Department of Biochemistry, Faculty of Medicine, University of Khartoum, Khartoum, Sudan
5Department of Basic Medical Sciences, Faculty of Dentistry, University of Khartoum, Khartoum, Sudan

Correspondence should be addressed to Mutaz Amin; ku.oc.liamtoh@88ztm

Received 23 April 2017; Revised 4 July 2017; Accepted 11 July 2017; Published 6 December 2017

Academic Editor: Xinhua Shu

Copyright © 2017 Hazem Kaheel et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Hazem Kaheel, Andreas Breß, Mohamed A. Hassan, et al., “Frequency of c.35delG Mutation in GJB2 Gene (Connexin 26) in Syrian Patients with Nonsyndromic Hearing Impairment,” Genetics Research International, vol. 2017, Article ID 5836525, 3 pages, 2017. https://doi.org/10.1155/2017/5836525.