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Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
| Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Nature Publishing Group UK
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318025/ https://www.ncbi.nlm.nih.gov/pubmed/37400429 http://dx.doi.org/10.1038/s41467-023-39492-4 |
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| author | Oddsson, Asmundur Sulem, Patrick Sveinbjornsson, Gardar Arnadottir, Gudny A. Steinthorsdottir, Valgerdur Halldorsson, Gisli H. Atlason, Bjarni A. Oskarsson, Gudjon R. Helgason, Hannes Nielsen, Henriette Svarre Westergaard, David Karjalainen, Juha M. Katrinardottir, Hildigunnur Fridriksdottir, Run Jensson, Brynjar O. Tragante, Vinicius Ferkingstad, Egil Jonsson, Hakon Gudjonsson, Sigurjon A. Beyter, Doruk Moore, Kristjan H. S. Thordardottir, Helga B. Kristmundsdottir, Snaedis Stefansson, Olafur A. Rantapää-Dahlqvist, Solbritt Sonderby, Ida Elken Didriksen, Maria Stridh, Pernilla Haavik, Jan Tryggvadottir, Laufey Frei, Oleksandr Walters, G. Bragi Kockum, Ingrid Hjalgrim, Henrik Olafsdottir, Thorunn A. Selbaek, Geir Nyegaard, Mette Erikstrup, Christian Brodersen, Thorsten Saevarsdottir, Saedis Olsson, Tomas Nielsen, Kaspar Rene Haraldsson, Asgeir Bruun, Mie Topholm Hansen, Thomas Folkmann Steingrimsdottir, Thora Jacobsen, Rikke Louise Lie, Rolv T. Djurovic, Srdjan Alfredsson, Lars Lopez de Lapuente Portilla, Aitzkoa Brunak, Soren Melsted, Pall Halldorsson, Bjarni V. Saemundsdottir, Jona Magnusson, Olafur Th. Padyukov, Leonid Banasik, Karina Rafnar, Thorunn Askling, Johan Klareskog, Lars Pedersen, Ole Birger Masson, Gisli Havdahl, Alexandra Nilsson, Bjorn Andreassen, Ole A. Daly, Mark Ostrowski, Sisse Rye Jonsdottir, Ingileif Stefansson, Hreinn Holm, Hilma Helgason, Agnar Thorsteinsdottir, Unnur Stefansson, Kari Gudbjartsson, Daniel F. |
| author_facet | Oddsson, Asmundur Sulem, Patrick Sveinbjornsson, Gardar Arnadottir, Gudny A. Steinthorsdottir, Valgerdur Halldorsson, Gisli H. Atlason, Bjarni A. Oskarsson, Gudjon R. Helgason, Hannes Nielsen, Henriette Svarre Westergaard, David Karjalainen, Juha M. Katrinardottir, Hildigunnur Fridriksdottir, Run Jensson, Brynjar O. Tragante, Vinicius Ferkingstad, Egil Jonsson, Hakon Gudjonsson, Sigurjon A. Beyter, Doruk Moore, Kristjan H. S. Thordardottir, Helga B. Kristmundsdottir, Snaedis Stefansson, Olafur A. Rantapää-Dahlqvist, Solbritt Sonderby, Ida Elken Didriksen, Maria Stridh, Pernilla Haavik, Jan Tryggvadottir, Laufey Frei, Oleksandr Walters, G. Bragi Kockum, Ingrid Hjalgrim, Henrik Olafsdottir, Thorunn A. Selbaek, Geir Nyegaard, Mette Erikstrup, Christian Brodersen, Thorsten Saevarsdottir, Saedis Olsson, Tomas Nielsen, Kaspar Rene Haraldsson, Asgeir Bruun, Mie Topholm Hansen, Thomas Folkmann Steingrimsdottir, Thora Jacobsen, Rikke Louise Lie, Rolv T. Djurovic, Srdjan Alfredsson, Lars Lopez de Lapuente Portilla, Aitzkoa Brunak, Soren Melsted, Pall Halldorsson, Bjarni V. Saemundsdottir, Jona Magnusson, Olafur Th. Padyukov, Leonid Banasik, Karina Rafnar, Thorunn Askling, Johan Klareskog, Lars Pedersen, Ole Birger Masson, Gisli Havdahl, Alexandra Nilsson, Bjorn Andreassen, Ole A. Daly, Mark Ostrowski, Sisse Rye Jonsdottir, Ingileif Stefansson, Hreinn Holm, Hilma Helgason, Agnar Thorsteinsdottir, Unnur Stefansson, Kari Gudbjartsson, Daniel F. |
| author_sort | Oddsson, Asmundur |
| collection | PubMed |
| description | |
| format | Online Article Text |
| id | pubmed-10318025 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2023 |
| publisher | Nature Publishing Group UK |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-103180252023-07-05 Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality Oddsson, Asmundur Sulem, Patrick Sveinbjornsson, Gardar Arnadottir, Gudny A. Steinthorsdottir, Valgerdur Halldorsson, Gisli H. Atlason, Bjarni A. Oskarsson, Gudjon R. Helgason, Hannes Nielsen, Henriette Svarre Westergaard, David Karjalainen, Juha M. Katrinardottir, Hildigunnur Fridriksdottir, Run Jensson, Brynjar O. Tragante, Vinicius Ferkingstad, Egil Jonsson, Hakon Gudjonsson, Sigurjon A. Beyter, Doruk Moore, Kristjan H. S. Thordardottir, Helga B. Kristmundsdottir, Snaedis Stefansson, Olafur A. Rantapää-Dahlqvist, Solbritt Sonderby, Ida Elken Didriksen, Maria Stridh, Pernilla Haavik, Jan Tryggvadottir, Laufey Frei, Oleksandr Walters, G. Bragi Kockum, Ingrid Hjalgrim, Henrik Olafsdottir, Thorunn A. Selbaek, Geir Nyegaard, Mette Erikstrup, Christian Brodersen, Thorsten Saevarsdottir, Saedis Olsson, Tomas Nielsen, Kaspar Rene Haraldsson, Asgeir Bruun, Mie Topholm Hansen, Thomas Folkmann Steingrimsdottir, Thora Jacobsen, Rikke Louise Lie, Rolv T. Djurovic, Srdjan Alfredsson, Lars Lopez de Lapuente Portilla, Aitzkoa Brunak, Soren Melsted, Pall Halldorsson, Bjarni V. Saemundsdottir, Jona Magnusson, Olafur Th. Padyukov, Leonid Banasik, Karina Rafnar, Thorunn Askling, Johan Klareskog, Lars Pedersen, Ole Birger Masson, Gisli Havdahl, Alexandra Nilsson, Bjorn Andreassen, Ole A. Daly, Mark Ostrowski, Sisse Rye Jonsdottir, Ingileif Stefansson, Hreinn Holm, Hilma Helgason, Agnar Thorsteinsdottir, Unnur Stefansson, Kari Gudbjartsson, Daniel F. Nat Commun Publisher Correction Nature Publishing Group UK 2023-07-03 /pmc/articles/PMC10318025/ /pubmed/37400429 http://dx.doi.org/10.1038/s41467-023-39492-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
| spellingShingle | Publisher Correction Oddsson, Asmundur Sulem, Patrick Sveinbjornsson, Gardar Arnadottir, Gudny A. Steinthorsdottir, Valgerdur Halldorsson, Gisli H. Atlason, Bjarni A. Oskarsson, Gudjon R. Helgason, Hannes Nielsen, Henriette Svarre Westergaard, David Karjalainen, Juha M. Katrinardottir, Hildigunnur Fridriksdottir, Run Jensson, Brynjar O. Tragante, Vinicius Ferkingstad, Egil Jonsson, Hakon Gudjonsson, Sigurjon A. Beyter, Doruk Moore, Kristjan H. S. Thordardottir, Helga B. Kristmundsdottir, Snaedis Stefansson, Olafur A. Rantapää-Dahlqvist, Solbritt Sonderby, Ida Elken Didriksen, Maria Stridh, Pernilla Haavik, Jan Tryggvadottir, Laufey Frei, Oleksandr Walters, G. Bragi Kockum, Ingrid Hjalgrim, Henrik Olafsdottir, Thorunn A. Selbaek, Geir Nyegaard, Mette Erikstrup, Christian Brodersen, Thorsten Saevarsdottir, Saedis Olsson, Tomas Nielsen, Kaspar Rene Haraldsson, Asgeir Bruun, Mie Topholm Hansen, Thomas Folkmann Steingrimsdottir, Thora Jacobsen, Rikke Louise Lie, Rolv T. Djurovic, Srdjan Alfredsson, Lars Lopez de Lapuente Portilla, Aitzkoa Brunak, Soren Melsted, Pall Halldorsson, Bjarni V. Saemundsdottir, Jona Magnusson, Olafur Th. Padyukov, Leonid Banasik, Karina Rafnar, Thorunn Askling, Johan Klareskog, Lars Pedersen, Ole Birger Masson, Gisli Havdahl, Alexandra Nilsson, Bjorn Andreassen, Ole A. Daly, Mark Ostrowski, Sisse Rye Jonsdottir, Ingileif Stefansson, Hreinn Holm, Hilma Helgason, Agnar Thorsteinsdottir, Unnur Stefansson, Kari Gudbjartsson, Daniel F. Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality |
| title | Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality |
| title_full | Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality |
| title_fullStr | Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality |
| title_full_unstemmed | Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality |
| title_short | Publisher Correction: Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality |
| title_sort | publisher correction: deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality |
| topic | Publisher Correction |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318025/ https://www.ncbi.nlm.nih.gov/pubmed/37400429 http://dx.doi.org/10.1038/s41467-023-39492-4 |
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