Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease.
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- Record sourced from PubMed, PMID 30607024.
- Also identified by DOI 10.1038/s41436-018-0392-y and PMC identifier 6752296.
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Abstract
The original version of this Article contained an incorrect version of Fig. 3, which included two variants initially shown in black text in Fig. 3a that the authors removed from the final manuscript. The correct version of Fig. 3 without the two variants now appears in the PDF and HTML versions of the Article.