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. 2018 Oct 8;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

Kristof Van Schil 1, Sarah Naessens 1, Stijn Van de Sompele 1, Marjolein Carron 1, Alexander Aslanidis 2, Caroline Van Cauwenbergh 1, Anja K Mayer 3, Mattias Van Heetvelde 1, Miriam Bauwens 1, Hannah Verdin 1, Frauke Coppieters 1, Michael E Greenberg 4, Marty G Yang 4, Marcus Karlstetter 2, Thomas Langmann 2, Katleen De Preter 1, Susanne Kohl 3, Timothy J Cherry 5,6, Bart P Leroy 1,7,8; CNV Study Group, Elfride De Baere 1,
PMCID: PMC7609298  PMID: 30297699

Correction to: Genetics in Medicine; 10.1038/gim.2017.97; published online 27 July 2017

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.

Footnotes

The CNV Study Group members and their affiliations are listed after Acknowledgments.

Contributor Information

Elfride De Baere, Email: Elfride.DeBaere@UGent.be.

CNV Study Group:

James R Lupski, Claudia Carvalho, Max van Min, Petra Klous, Sarah De Jaegere, and Sally Hooghe


Articles from Genetics in Medicine are provided here courtesy of Nature Publishing Group

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