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Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects
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/PMC10272200/ https://www.ncbi.nlm.nih.gov/pubmed/37322043 http://dx.doi.org/10.1038/s41467-023-39372-x |
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author | Ayers, Katie L. Eggers, Stefanie Rollo, Ben N. Smith, Katherine R. Davidson, Nadia M. Siddall, Nicole A. Zhao, Liang Bowles, Josephine Weiss, Karin Zanni, Ginevra Burglen, Lydie Ben-Shachar, Shay Rosensaft, Jenny Raas-Rothschild, Annick Jørgensen, Anne Schittenhelm, Ralf B. Huang, Cheng Robevska, Gorjana van den Bergen, Jocelyn Casagranda, Franca Cyza, Justyna Pachernegg, Svenja Wright, David K. Bahlo, Melanie Oshlack, Alicia O’Brien, Terrence J. Kwan, Patrick Koopman, Peter Hime, Gary R. Girard, Nadine Hoffmann, Chen Shilon, Yuval Zung, Amnon Bertini, Enrico Milh, Mathieu Ben Rhouma, Bochra Belguith, Neila Bashamboo, Anu McElreavey, Kenneth Banne, Ehud Weintrob, Naomi BenZeev, Bruria Sinclair, Andrew H. |
author_facet | Ayers, Katie L. Eggers, Stefanie Rollo, Ben N. Smith, Katherine R. Davidson, Nadia M. Siddall, Nicole A. Zhao, Liang Bowles, Josephine Weiss, Karin Zanni, Ginevra Burglen, Lydie Ben-Shachar, Shay Rosensaft, Jenny Raas-Rothschild, Annick Jørgensen, Anne Schittenhelm, Ralf B. Huang, Cheng Robevska, Gorjana van den Bergen, Jocelyn Casagranda, Franca Cyza, Justyna Pachernegg, Svenja Wright, David K. Bahlo, Melanie Oshlack, Alicia O’Brien, Terrence J. Kwan, Patrick Koopman, Peter Hime, Gary R. Girard, Nadine Hoffmann, Chen Shilon, Yuval Zung, Amnon Bertini, Enrico Milh, Mathieu Ben Rhouma, Bochra Belguith, Neila Bashamboo, Anu McElreavey, Kenneth Banne, Ehud Weintrob, Naomi BenZeev, Bruria Sinclair, Andrew H. |
author_sort | Ayers, Katie L. |
collection | PubMed |
description | |
format | Online Article Text |
id | pubmed-10272200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102722002023-06-17 Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects Ayers, Katie L. Eggers, Stefanie Rollo, Ben N. Smith, Katherine R. Davidson, Nadia M. Siddall, Nicole A. Zhao, Liang Bowles, Josephine Weiss, Karin Zanni, Ginevra Burglen, Lydie Ben-Shachar, Shay Rosensaft, Jenny Raas-Rothschild, Annick Jørgensen, Anne Schittenhelm, Ralf B. Huang, Cheng Robevska, Gorjana van den Bergen, Jocelyn Casagranda, Franca Cyza, Justyna Pachernegg, Svenja Wright, David K. Bahlo, Melanie Oshlack, Alicia O’Brien, Terrence J. Kwan, Patrick Koopman, Peter Hime, Gary R. Girard, Nadine Hoffmann, Chen Shilon, Yuval Zung, Amnon Bertini, Enrico Milh, Mathieu Ben Rhouma, Bochra Belguith, Neila Bashamboo, Anu McElreavey, Kenneth Banne, Ehud Weintrob, Naomi BenZeev, Bruria Sinclair, Andrew H. Nat Commun Author Correction Nature Publishing Group UK 2023-06-15 /pmc/articles/PMC10272200/ /pubmed/37322043 http://dx.doi.org/10.1038/s41467-023-39372-x 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 | Author Correction Ayers, Katie L. Eggers, Stefanie Rollo, Ben N. Smith, Katherine R. Davidson, Nadia M. Siddall, Nicole A. Zhao, Liang Bowles, Josephine Weiss, Karin Zanni, Ginevra Burglen, Lydie Ben-Shachar, Shay Rosensaft, Jenny Raas-Rothschild, Annick Jørgensen, Anne Schittenhelm, Ralf B. Huang, Cheng Robevska, Gorjana van den Bergen, Jocelyn Casagranda, Franca Cyza, Justyna Pachernegg, Svenja Wright, David K. Bahlo, Melanie Oshlack, Alicia O’Brien, Terrence J. Kwan, Patrick Koopman, Peter Hime, Gary R. Girard, Nadine Hoffmann, Chen Shilon, Yuval Zung, Amnon Bertini, Enrico Milh, Mathieu Ben Rhouma, Bochra Belguith, Neila Bashamboo, Anu McElreavey, Kenneth Banne, Ehud Weintrob, Naomi BenZeev, Bruria Sinclair, Andrew H. Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects |
title | Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects |
title_full | Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects |
title_fullStr | Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects |
title_full_unstemmed | Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects |
title_short | Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects |
title_sort | author correction: variants in sart3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects |
topic | Author Correction |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10272200/ https://www.ncbi.nlm.nih.gov/pubmed/37322043 http://dx.doi.org/10.1038/s41467-023-39372-x |
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