Author
Listed:
- Katie L. Ayers
(The Murdoch Children’s Research Institute
The University of Melbourne)
- Stefanie Eggers
(The Victorian Clinical Genetics Services)
- Ben N. Rollo
(Monash University, Alfred Centre)
- Katherine R. Smith
(Walter and Eliza Hall Institute of Medical Research)
- Nadia M. Davidson
(Walter and Eliza Hall Institute of Medical Research
Faculty of Science, University of Melbourne
University of Melbourne)
- Nicole A. Siddall
(The University of Melbourne)
- Liang Zhao
(The University of Queensland)
- Josephine Bowles
(The University of Queensland
The University of Queensland)
- Karin Weiss
(Rappaport Faculty of Medicine, Institute of Technology)
- Ginevra Zanni
(Bambino Gesù Children’s Hospital, IRCCS)
- Lydie Burglen
(APHP. Sorbonne Université, Hôpital Trousseau
Developmental Brain Disorders Laboratory, Imagine Institute)
- Shay Ben-Shachar
(Genetic Institute, Tel Aviv Sourasky Medical Center)
- Jenny Rosensaft
(Hebrew University Hadassah Medical School)
- Annick Raas-Rothschild
(Edmond and Lily Safra Children’s Hospital, Chaim Sheba Medical Center
Tel Aviv University)
- Anne Jørgensen
(Copenhagen University Hospital, Rigshospitalet)
- Ralf B. Schittenhelm
(Monash University)
- Cheng Huang
(Monash University)
- Gorjana Robevska
(The Murdoch Children’s Research Institute)
- Jocelyn van den Bergen
(The Murdoch Children’s Research Institute)
- Franca Casagranda
(The University of Melbourne)
- Justyna Cyza
(The Murdoch Children’s Research Institute)
- Svenja Pachernegg
(The Murdoch Children’s Research Institute
The University of Melbourne)
- David K. Wright
(Monash University, Alfred Centre)
- Melanie Bahlo
(Walter and Eliza Hall Institute of Medical Research
University of Melbourne)
- Alicia Oshlack
(The Peter MacCallum Cancer Centre
The University of Melbourne)
- Terrence J. O’Brien
(Monash University, Alfred Centre
The University of Melbourne)
- Patrick Kwan
(Monash University, Alfred Centre
The University of Melbourne)
- Peter Koopman
(The University of Queensland)
- Gary R. Hime
(The University of Melbourne)
- Nadine Girard
(Aix-Marseille Université, APHM, Timone Hospital)
- Chen Hoffmann
(Sheba medical Centre)
- Yuval Shilon
(Hebrew University Hadassah Medical School)
- Amnon Zung
(Kaplan Medical Center
Hebrew University of Jerusalem, Hadassah Medical School)
- Enrico Bertini
(Bambino Gesù Children’s Hospital, IRCCS)
- Mathieu Milh
(Aix-Marseille Université, APHM, Timone Hospital)
- Bochra Ben Rhouma
(University of Gabes
Sfax University)
- Neila Belguith
(Sfax University
Charles Nicolle Hospital)
- Anu Bashamboo
(Institut Pasteur, Université de Paris, CNRS UMR3738, Human Developmental Genetics)
- Kenneth McElreavey
(Institut Pasteur, Université de Paris, CNRS UMR3738, Human Developmental Genetics)
- Ehud Banne
(Hebrew University Hadassah Medical School
The Rina Mor Genetic Institute, Wolfson Medical Center)
- Naomi Weintrob
(Tel Aviv University
Dana-Dwek Children’s Hospital, Tel Aviv Medical Center)
- Bruria BenZeev
(Sheba Medical Center)
- Andrew H. Sinclair
(The Murdoch Children’s Research Institute
The University of Melbourne)
Abstract
No abstract is available for this item.
Suggested Citation
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-Sh, 2023.
"Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects,"
Nature Communications, Nature, vol. 14(1), pages 1-1, December.
Handle:
RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-39372-x
DOI: 10.1038/s41467-023-39372-x
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