![Man ultramarathon runner in the mountains he trains at sunset](https://d2csxpduxe849s.cloudfront.net/media/E32629C6-9347-4F84-81FEAEF7BFA342B3/0B4B1380-42EB-4FD5-9D7E2DBC603E79F8/webimage-C4875379-1478-416F-B03DF68FE3D8DBB5.png)
94% of researchers rate our articles as excellent or good
Learn more about the work of our research integrity team to safeguard the quality of each article we publish.
Find out more
CORRECTION article
Front. Genet. , 25 January 2023
Sec. Genetics of Common and Rare Diseases
Volume 14 - 2023 | https://doi.org/10.3389/fgene.2023.1143795
This article is a correction to:
Spondyloocular Syndrome: A Novel XYLT2 Variant with Description of the Neonatal Phenotype
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.
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
Disclaimer: 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.
Research integrity at Frontiers
Learn more about the work of our research integrity team to safeguard the quality of each article we publish.