Statistics from Altmetric.com
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.
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.