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Gabriella Doddato1,2†Alessandra Fabbiani1,2,3†Chiara Fallerini1,2
Mirella Bruttini1,2,3Theodora Hadjistilianou4Martino Landi5Caterina Coradeschi5
Salvatore Grosso6Barbara Tomasini5Maria Antonietta Mencarelli3
Alessandra Renieri1,2,3Francesca Ariani1,2,3*- 1Medical Genetics, University of Siena, Siena, Tuscany, Italy
- 2Med Biotech Hub and Competence Center, Department of Medical Biotechnologies, University of Siena, Siena, Tuscany, Italy
- 3Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy
- 4Ophthalmological Science and Neuroscience, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy
- 5Terapia Intensiva Neonatale, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy
- 6Pediatria, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy
A Corrigendum on
Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype
by Doddato G, Fabbiani A, Fallerini C, Bruttini M, Hadjistilianou T, Landi M, Coradeschi C, Grosso S, Tomasini B, Mencarelli MA, Renieri A and Ariani F (2021). Front. Genet. 12:761264. doi: 10.3389/fgene.2021.761264
In the published article, there was an error. There was a sentence missing in the Acknowledgments section.
A correction has been made to the Acknowledgments. This sentence previously stated:
“The authors thank the family for participating in the study.”
The corrected sentence appears below:
“The authors thank the family for participating in the study. Two of the authors of this publication are members of the European Reference Network for rare malformation syndromes and rare intellectual and neurodevelopmental disorders, ERN-ITHACA.”
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Keywords: spondyloocular syndrome (SOS), xylosyltransferase II, Exome Sequencing (ES), skeletal dysplasia, XYLT2
Citation: Doddato G, Fabbiani A, Fallerini C, Bruttini M, Hadjistilianou T, Landi M, Coradeschi C, Grosso S, Tomasini B, Mencarelli MA, Renieri A and Ariani F (2023) Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype. Front. Genet. 14:1143795. doi: 10.3389/fgene.2023.1143795
Received: 13 January 2023; Accepted: 16 January 2023;
Published: 25 January 2023.
Approved by:
Frontiers Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2023 Doddato, Fabbiani, Fallerini, Bruttini, Hadjistilianou, Landi, Coradeschi, Grosso, Tomasini, Mencarelli, Renieri and Ariani. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Francesca Ariani, ZnJhbmNlc2NhLmFyaWFuaUB1bmlzaS5pdA==
†These authors have contributed equally to this work and share first authorship