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Genetics Research International
Volume 2011, Article ID 368915, 4 pages
http://dx.doi.org/10.4061/2011/368915
Research Article

A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families

1Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Tx 77030, USA
2Department of Biochemistry, Faculty of Biological Sciences, Quaid-I-Azam University, Islamabad 45320, Pakistan

Received 30 May 2011; Accepted 1 August 2011

Academic Editor: Karen Friderici

Copyright © 2011 Kwanghyuk Lee 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

Kwanghyuk Lee, Saadullah Khan, Muhammad Ansar, Regie Lyn P. Santos-Cortez, Wasim Ahmad, and Suzanne M. Leal, “A Novel ESRRB Deletion Is a Rare Cause of Autosomal Recessive Nonsyndromic Hearing Impairment among Pakistani Families,” Genetics Research International, vol. 2011, Article ID 368915, 4 pages, 2011. https://doi.org/10.4061/2011/368915.