Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects
| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2023-06-01
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| Series: | Nature Communications |
| Online Access: | https://doi.org/10.1038/s41467-023-39372-x |
| _version_ | 1827922929317314560 |
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| author | Katie L. Ayers Stefanie Eggers Ben N. Rollo Katherine R. Smith Nadia M. Davidson Nicole A. Siddall Liang Zhao Josephine Bowles Karin Weiss Ginevra Zanni Lydie Burglen Shay Ben-Shachar Jenny Rosensaft Annick Raas-Rothschild Anne Jørgensen Ralf B. Schittenhelm Cheng Huang Gorjana Robevska Jocelyn van den Bergen Franca Casagranda Justyna Cyza Svenja Pachernegg David K. Wright Melanie Bahlo Alicia Oshlack Terrence J. O’Brien Patrick Kwan Peter Koopman Gary R. Hime Nadine Girard Chen Hoffmann Yuval Shilon Amnon Zung Enrico Bertini Mathieu Milh Bochra Ben Rhouma Neila Belguith Anu Bashamboo Kenneth McElreavey Ehud Banne Naomi Weintrob Bruria BenZeev Andrew H. Sinclair |
| author_facet | Katie L. Ayers Stefanie Eggers Ben N. Rollo Katherine R. Smith Nadia M. Davidson Nicole A. Siddall Liang Zhao Josephine Bowles Karin Weiss Ginevra Zanni Lydie Burglen Shay Ben-Shachar Jenny Rosensaft Annick Raas-Rothschild Anne Jørgensen Ralf B. Schittenhelm Cheng Huang Gorjana Robevska Jocelyn van den Bergen Franca Casagranda Justyna Cyza Svenja Pachernegg David K. Wright Melanie Bahlo Alicia Oshlack Terrence J. O’Brien Patrick Kwan Peter Koopman Gary R. Hime Nadine Girard Chen Hoffmann Yuval Shilon Amnon Zung Enrico Bertini Mathieu Milh Bochra Ben Rhouma Neila Belguith Anu Bashamboo Kenneth McElreavey Ehud Banne Naomi Weintrob Bruria BenZeev Andrew H. Sinclair |
| author_sort | Katie L. Ayers |
| collection | DOAJ |
| first_indexed | 2024-03-13T04:49:20Z |
| format | Article |
| id | doaj.art-4d17ed3fcc1b46bc9b7e947038dedff7 |
| institution | Directory Open Access Journal |
| issn | 2041-1723 |
| language | English |
| last_indexed | 2024-03-13T04:49:20Z |
| publishDate | 2023-06-01 |
| publisher | Nature Portfolio |
| record_format | Article |
| series | Nature Communications |
| spelling | doaj.art-4d17ed3fcc1b46bc9b7e947038dedff72023-06-18T11:18:09ZengNature PortfolioNature Communications2041-17232023-06-011411110.1038/s41467-023-39372-xAuthor Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defectsKatie L. Ayers0Stefanie Eggers1Ben N. Rollo2Katherine R. Smith3Nadia M. Davidson4Nicole A. Siddall5Liang Zhao6Josephine Bowles7Karin Weiss8Ginevra Zanni9Lydie Burglen10Shay Ben-Shachar11Jenny Rosensaft12Annick Raas-Rothschild13Anne Jørgensen14Ralf B. Schittenhelm15Cheng Huang16Gorjana Robevska17Jocelyn van den Bergen18Franca Casagranda19Justyna Cyza20Svenja Pachernegg21David K. Wright22Melanie Bahlo23Alicia Oshlack24Terrence J. O’Brien25Patrick Kwan26Peter Koopman27Gary R. Hime28Nadine Girard29Chen Hoffmann30Yuval Shilon31Amnon Zung32Enrico Bertini33Mathieu Milh34Bochra Ben Rhouma35Neila Belguith36Anu Bashamboo37Kenneth McElreavey38Ehud Banne39Naomi Weintrob40Bruria BenZeev41Andrew H. Sinclair42The Murdoch Children’s Research InstituteThe Victorian Clinical Genetics ServicesDepartment of Neuroscience, Central Clinical School, Monash University, Alfred CentreWalter and Eliza Hall Institute of Medical ResearchWalter and Eliza Hall Institute of Medical ResearchDepartment of Anatomy and Physiology, The University of MelbourneInstitute for Molecular Bioscience, The University of QueenslandInstitute for Molecular Bioscience, The University of QueenslandGenetics Institute, Rambam Health Care Campus, Rappaport Faculty of Medicine, Institute of TechnologyUnit of Muscular and Neurodegenerative Disorders and Unit of Developmental Neurology, Department of Neurosciences, Bambino Gesù Children’s Hospital, IRCCSCentre de Référence des Malformations et Maladies Congénitales du Cervelet, Et Laboratoire de Neurogénétique Moléculaire, Département de Génétique et Embryologie Médicale, APHP. Sorbonne Université, Hôpital TrousseauGenetic Institute, Tel Aviv Sourasky Medical CenterGenetics Institute, Kaplan Medical Center, Hebrew University Hadassah Medical SchoolEdmond and Lily Safra Children’s Hospital, Chaim Sheba Medical CenterDepartment of Growth and Reproduction, Copenhagen University Hospital, RigshospitaletMonash Proteomics and Metabolomics Facility, Biomedicine Discovery Institute, Department of Biochemistry and Molecular Biology, Monash UniversityMonash Proteomics and Metabolomics Facility, Biomedicine Discovery Institute, Department of Biochemistry and Molecular Biology, Monash UniversityThe Murdoch Children’s Research InstituteThe Murdoch Children’s Research InstituteDepartment of Anatomy and Physiology, The University of MelbourneThe Murdoch Children’s Research InstituteThe Murdoch Children’s Research InstituteDepartment of Neuroscience, Central Clinical School, Monash University, Alfred CentreWalter and Eliza Hall Institute of Medical ResearchThe Peter MacCallum Cancer CentreDepartment of Neuroscience, Central Clinical School, Monash University, Alfred CentreDepartment of Neuroscience, Central Clinical School, Monash University, Alfred CentreInstitute for Molecular Bioscience, The University of QueenslandDepartment of Anatomy and Physiology, The University of MelbourneDepartment of Pediatric Neurology, Aix-Marseille Université, APHM, Timone HospitalRadiology Department, Sheba medical CentreKaplan Medical Center, Hebrew University Hadassah Medical SchoolPediatrics Department, Kaplan Medical CenterUnit of Muscular and Neurodegenerative Disorders and Unit of Developmental Neurology, Department of Neurosciences, Bambino Gesù Children’s Hospital, IRCCSDepartment of Pediatric Neurology, Aix-Marseille Université, APHM, Timone HospitalHigher Institute of Nursing Sciences of Gabes, University of GabesLaboratory of Human Molecular Genetics, Faculty of Medicine of Sfax, Sfax UniversityInstitut Pasteur, Université de Paris, CNRS UMR3738, Human Developmental GeneticsInstitut Pasteur, Université de Paris, CNRS UMR3738, Human Developmental GeneticsGenetics Institute, Kaplan Medical Center, Hebrew University Hadassah Medical SchoolSackler School of Medicine, Tel Aviv UniversitySheba Medical CenterThe Murdoch Children’s Research Institutehttps://doi.org/10.1038/s41467-023-39372-x |
| spellingShingle | Katie L. Ayers Stefanie Eggers Ben N. Rollo Katherine R. Smith Nadia M. Davidson Nicole A. Siddall Liang Zhao Josephine Bowles Karin Weiss Ginevra Zanni Lydie Burglen Shay Ben-Shachar Jenny Rosensaft Annick Raas-Rothschild Anne Jørgensen Ralf B. Schittenhelm Cheng Huang Gorjana Robevska Jocelyn van den Bergen Franca Casagranda Justyna Cyza Svenja Pachernegg David K. Wright Melanie Bahlo Alicia Oshlack Terrence J. O’Brien Patrick Kwan Peter Koopman Gary R. Hime Nadine Girard Chen Hoffmann Yuval Shilon Amnon Zung Enrico Bertini Mathieu Milh Bochra Ben Rhouma Neila Belguith Anu Bashamboo Kenneth McElreavey Ehud Banne Naomi Weintrob Bruria BenZeev Andrew H. Sinclair Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects Nature Communications |
| 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 |
| url | https://doi.org/10.1038/s41467-023-39372-x |
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