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Published Erratum
. 2016 Mar 31;11(3):e0153121.
doi: 10.1371/journal.pone.0153121. eCollection 2016.

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
Published Erratum

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

Marta Corton et al. PLoS One. .
No abstract available

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Figures

Fig 1
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.
See this image and copyright information in PMC

Erratum for

References

    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 doi: 10.1371/journal.pone.0065574 - DOI - PMC - PubMed

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