The affiliation for the 6th author is missing. Nejat Mahdieh is affiliated with #3. Affiliation #3 was incomplete in the PDF document. Affiliation number 3 is: Growth and Development Research Center, Tehran University of Medical Sciences, Tehran and Faculty of Medicine, Ilam University of Medical Sciences, Ilam, Iran
Citation: Diaz-Horta O, Duman D, Foster J II, Sırmacı A, Gonzalez M, Mahdieh N, et al. (2013) Correction: Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss. PLoS ONE 8(5): 10.1371/annotation/0668e8de-97ae-4a04-ac61-8afa9c79bbdd. doi:10.1371/annotation/0668e8de-97ae-4a04-ac61-8afa9c79bbdd
Published: May 17, 2013
Copyright: © 2013 . This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Competing interests: No competing interests declared.