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Correction: Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions
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Kumaran N, Moore AT, Weleber RG, et al. Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions. Br J Ophthalmol 2017;101:1147–54. doi: 10.1136/bjophthalmol-2016-309975.
The authors wish to correct the legend of table 1. It reads: *Genes associated with EOSRD. †Genes more frequently associated with LCA. However it should read: †Genes associated with EOSRD. *Genes more frequently associated with LCA.
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© Author(s) (or their employer(s)) 2019. Re-usepermitted under CC BY. Published by BMJ. This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by/4.0/