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Genet Med. 2019 Aug;21(8):1998. doi: 10.1038/s41436-018-0305-0.

Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations.

Author information

1
Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium.
2
Laboratory for Experimental Immunology of the Eye, Department of Ophthalmology, University of Cologne, Cologne, Germany.
3
Molecular Genetics Laboratory, Institute for Ophthalmic Research, Centre for Ophthalmology, University of Tuebingen, Tuebingen, Germany.
4
Department of Neurobiology, Harvard Medical School, Boston, Massachusetts, USA.
5
Department of Pediatrics, University of Washington School of Medicine, Seattle, Washington, USA.
6
Center for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, Washington, USA.
7
Department of Ophthalmology, Ghent University and Ghent University Hospital, Ghent, Belgium.
8
Division of Ophthalmology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
9
Center for Medical Genetics, Ghent University and Ghent University Hospital, Ghent, Belgium. Elfride.DeBaere@UGent.be.

Abstract

The original version of this Article contained an error in the spelling of the author Anja K. Mayer, which was incorrectly given as Anja Kathrin Mayer. This has now been corrected in both the PDF and HTML versions of the Article.

PMID:
30297699
DOI:
10.1038/s41436-018-0305-0

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