This Article contains errors. The position of the mutation p.(R91W); (V172D) was incorrectly calculated, taking as a starting point the beginning of cDNA rather than the start codon. The correct position of the mutation is c.[271C > T]; [515T > A]. As a result of this the following changes in the Article are made:
The legend of Figure 3 is incorrect,
“(C) c.[325C > T]; [569T > A] (RPE65)”
should read:
“(C) c.[271C > T]; [515T > A] (RPE65)”.
In Table 3 for the family ID F7, the DNA mutation should read ‘c.[271C > T]; [515T > A]’.
In Figure 5 for family F7 ‘RPE65, c.325C > T; 569T > A; p.R91W; V172D’ should read ‘RPE65, c.271C > T; 515T > A; p.R91W; V172D’. The correct Figure 5 appears below as Figure 1.
In the Results section under the subheading ‘Mutation analysis’,
“The second mutation was identified in family F7 and was a new compound heterozygous mutations c.[325C > T]; [569T > A] resulting in p.(R91W); (V172D) (Fig. 3C)”.
should read:
“The second mutation was identified in family F7 and was a new compound heterozygous mutations c.[271C > T]; [515T > A] resulting in p.(R91W); (V172D) (Fig. 3C)”.
Additional information
The online version of the original article can be found at 10.1038/srep37455
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Habibi, I., Chebil, A., Falfoul, Y. et al. Correction: Corrigendum: Identifying mutations in Tunisian families with retinal dystrophy. Sci Rep 7, 46776 (2017). https://doi.org/10.1038/srep46776
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DOI: https://doi.org/10.1038/srep46776
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