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Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease
| Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group US
2019
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752296/ https://www.ncbi.nlm.nih.gov/pubmed/30607024 http://dx.doi.org/10.1038/s41436-018-0392-y |
| _version_ | 1783452758559424512 |
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| author | Van de Sompele, Stijn Smith, Claire Karali, Marianthi Corton, Marta Van Schil, Kristof Peelman, Frank Cherry, Timothy Rosseel, Toon Verdin, Hannah Derolez, Julien Van Laethem, Thalia Khan, Kamron N. McKibbin, Martin Toomes, Carmel Ali, Manir Torella, Annalaura Testa, Francesco Jimenez, Belen Simonelli, Francesca De Zaeytijd, Julie Van den Ende, Jenneke Leroy, Bart P. Coppieters, Frauke Ayuso, Carmen Inglehearn, Chris F. Banfi, Sandro De Baere, Elfride |
| author_facet | Van de Sompele, Stijn Smith, Claire Karali, Marianthi Corton, Marta Van Schil, Kristof Peelman, Frank Cherry, Timothy Rosseel, Toon Verdin, Hannah Derolez, Julien Van Laethem, Thalia Khan, Kamron N. McKibbin, Martin Toomes, Carmel Ali, Manir Torella, Annalaura Testa, Francesco Jimenez, Belen Simonelli, Francesca De Zaeytijd, Julie Van den Ende, Jenneke Leroy, Bart P. Coppieters, Frauke Ayuso, Carmen Inglehearn, Chris F. Banfi, Sandro De Baere, Elfride |
| author_sort | Van de Sompele, Stijn |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-6752296 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2019 |
| publisher | Nature Publishing Group US |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-67522962019-09-23 Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease Van de Sompele, Stijn Smith, Claire Karali, Marianthi Corton, Marta Van Schil, Kristof Peelman, Frank Cherry, Timothy Rosseel, Toon Verdin, Hannah Derolez, Julien Van Laethem, Thalia Khan, Kamron N. McKibbin, Martin Toomes, Carmel Ali, Manir Torella, Annalaura Testa, Francesco Jimenez, Belen Simonelli, Francesca De Zaeytijd, Julie Van den Ende, Jenneke Leroy, Bart P. Coppieters, Frauke Ayuso, Carmen Inglehearn, Chris F. Banfi, Sandro De Baere, Elfride Genet Med Correction Nature Publishing Group US 2019-01-03 2019 /pmc/articles/PMC6752296/ /pubmed/30607024 http://dx.doi.org/10.1038/s41436-018-0392-y Text en © The Author(s) 2019 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/. |
| spellingShingle | Correction Van de Sompele, Stijn Smith, Claire Karali, Marianthi Corton, Marta Van Schil, Kristof Peelman, Frank Cherry, Timothy Rosseel, Toon Verdin, Hannah Derolez, Julien Van Laethem, Thalia Khan, Kamron N. McKibbin, Martin Toomes, Carmel Ali, Manir Torella, Annalaura Testa, Francesco Jimenez, Belen Simonelli, Francesca De Zaeytijd, Julie Van den Ende, Jenneke Leroy, Bart P. Coppieters, Frauke Ayuso, Carmen Inglehearn, Chris F. Banfi, Sandro De Baere, Elfride Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease |
| title | Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease |
| title_full | Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease |
| title_fullStr | Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease |
| title_full_unstemmed | Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease |
| title_short | Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease |
| title_sort | correction: biallelic sequence and structural variants in rax2 are a novel cause for autosomal recessive inherited retinal disease |
| topic | Correction |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752296/ https://www.ncbi.nlm.nih.gov/pubmed/30607024 http://dx.doi.org/10.1038/s41436-018-0392-y |
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