Correction: Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss. (PLoS ONE)

Oscar Diaz-Horta, Duygu Duman, Joseph Foster, Asli Sirmaci, Michael Gonzalez, Nejat Mahdieh, Nikou Fotouhi, Mortaza Bonyadi, Filiz Basa̧k Cengiz, Ibis Menendez, Rick H. Ulloa, Yvonne J.K. Edwards, Stephan Zuc̈hner, Susan Blanton, Mustafa Tekin

Research output: Contribution to journalComment/debate

Original languageEnglish (US)
JournalPloS one
Volume8
Issue number5
DOIs
StatePublished - May 17 2013
Externally publishedYes

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)
  • Agricultural and Biological Sciences(all)
  • General

Cite this

Diaz-Horta, O., Duman, D., Foster, J., Sirmaci, A., Gonzalez, M., Mahdieh, N., Fotouhi, N., Bonyadi, M., Cengiz, F. B., Menendez, I., Ulloa, R. H., Edwards, Y. J. K., Zuc̈hner, S., Blanton, S., & Tekin, M. (2013). Correction: Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss. (PLoS ONE). PloS one, 8(5). https://doi.org/10.1371/annotation/0668e8de-97ae-4a04-ac61-8afa9c79bbdd