Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease

Abstract

In addition, the Article was originally published under Nature Research's License to Publish but is now been made available under a CC BY-NC-ND 4.0 license. The authors have also requested the addition of an acknowledgement to the European Retinal Disease Consortium (ERDC). The PDF and HTML versions of the Article have been modified accordingly.