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author Van Schil, Kristof
Naessens, Sarah
Van de Sompele, Stijn
Carron, Marjolein
Aslanidis, Alexander
Van Cauwenbergh, Caroline
Mayer, Anja K.
Van Heetvelde, Mattias
Bauwens, Miriam
Verdin, Hannah
Coppieters, Frauke
Greenberg, Michael E.
Yang, Marty G.
Karlstetter, Marcus
Langmann, Thomas
De Preter, Katleen
Kohl, Susanne
Cherry, Timothy J.
Leroy, Bart P.
De Baere, Elfride
author_facet Van Schil, Kristof
Naessens, Sarah
Van de Sompele, Stijn
Carron, Marjolein
Aslanidis, Alexander
Van Cauwenbergh, Caroline
Mayer, Anja K.
Van Heetvelde, Mattias
Bauwens, Miriam
Verdin, Hannah
Coppieters, Frauke
Greenberg, Michael E.
Yang, Marty G.
Karlstetter, Marcus
Langmann, Thomas
De Preter, Katleen
Kohl, Susanne
Cherry, Timothy J.
Leroy, Bart P.
De Baere, Elfride
author_sort Van Schil, Kristof
collection PubMed
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spelling pubmed-76092982020-11-05 Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations Van Schil, Kristof Naessens, Sarah Van de Sompele, Stijn Carron, Marjolein Aslanidis, Alexander Van Cauwenbergh, Caroline Mayer, Anja K. Van Heetvelde, Mattias Bauwens, Miriam Verdin, Hannah Coppieters, Frauke Greenberg, Michael E. Yang, Marty G. Karlstetter, Marcus Langmann, Thomas De Preter, Katleen Kohl, Susanne Cherry, Timothy J. Leroy, Bart P. De Baere, Elfride Genet Med Correction Nature Publishing Group US 2018-10-08 2019 /pmc/articles/PMC7609298/ /pubmed/30297699 http://dx.doi.org/10.1038/s41436-018-0305-0 Text en © The Author(s) 2018 https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, and provide a link to the Creative Commons license. You do not have permission under this license to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Correction
Van Schil, Kristof
Naessens, Sarah
Van de Sompele, Stijn
Carron, Marjolein
Aslanidis, Alexander
Van Cauwenbergh, Caroline
Mayer, Anja K.
Van Heetvelde, Mattias
Bauwens, Miriam
Verdin, Hannah
Coppieters, Frauke
Greenberg, Michael E.
Yang, Marty G.
Karlstetter, Marcus
Langmann, Thomas
De Preter, Katleen
Kohl, Susanne
Cherry, Timothy J.
Leroy, Bart P.
De Baere, Elfride
Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
title Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
title_full Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
title_fullStr Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
title_full_unstemmed Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
title_short Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
title_sort correction: mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
topic Correction
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7609298/
https://www.ncbi.nlm.nih.gov/pubmed/30297699
http://dx.doi.org/10.1038/s41436-018-0305-0
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