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

Academic Article

Authors

Published In

  • PLoS ONE  Journal

    • Author List

  • Diaz-Horta O; Duman D; Foster J; Sirmaci A; Gonzalez M; Mahdieh N; Fotouhi N; Bonyadi M; Cengiz FB; Menendez I

    • Volume

  • 8

    • Issue

  • 5