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Open Access

Correction

Correction: Exome Sequencing of Index Patients with Retinal Dystrophies as a Tool for Molecular Diagnosis

  • Marta Corton,
  • Koji M. Nishiguchi,
  • Almudena Avila-Fernández,
  • Konstantinos Nikopoulos,
  • Rosa Riveiro-Alvarez,
  • Sorina D. Tatu,
  • Carmen Ayuso,
  • Carlo Rivolta
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There are two errors in the RP-1164 row and Nucleotide Change and Protein Change columns of Table 1. The mutation c.863dupA should be c.862dupA and the mutation p.M289Y*18 should be p.T288Nfs*19. There is also an error in Fig 1 under the panel RP-1164. The mutation p.M289Y*18 should be p.T288Nfs*19. Please view the correct Table 1 and Fig 1 here.

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Table 1. RD mutations identified by WES analyses.

https://doi.org/10.1371/journal.pone.0153121.t001

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Fig 1. Pedigrees of patients analyzed and mutations identified in this work.

The family ID is given above the pedigree, while the individuals’ IDs are indicated below the symbols depicting them. Red circles indicate individuals whose DNA underwent WES analysis. The name of the RD gene identified as causative of the disease is given in blue. M/M, homozygous mutation; M/m compound heterozygous mutations.

https://doi.org/10.1371/journal.pone.0153121.g001

Reference

  1. 1. Corton M, Nishiguchi KM, Avila-Fernández A, Nikopoulos K, Riveiro-Alvarez R, Tatu SD, et al. (2013) Exome Sequencing of Index Patients with Retinal Dystrophies as a Tool for Molecular Diagnosis. PLoS ONE 8(6): e65574. pmid:23940504

Citation: Corton M, Nishiguchi KM, Avila-Fernández A, Nikopoulos K, Riveiro-Alvarez R, Tatu SD, et al. (2016) Correction: Exome Sequencing of Index Patients with Retinal Dystrophies as a Tool for Molecular Diagnosis. PLoS ONE 11(3): e0153121. https://doi.org/10.1371/journal.pone.0153121

Published: March 31, 2016

Copyright: © 2016 Corton et al. 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.