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Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype.

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Affiliations

  • 1. Medical Genetics, University of Siena, Siena, Tuscany, Italy.
      Authors
    • Doddato G 1
    • Fabbiani A 1, 5
    • Fallerini C 1
    • Bruttini M 1, 5
    • Renieri A 1, 5
    • Ariani F 1, 5
    (6 authors)
  • 2. Ophthalmological Science and Neuroscience, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy.
      Authors
    • Hadjistilianou T 2
    (1 author)
  • 3. Terapia Intensiva Neonatale, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy.
      Authors
    • Landi M 3
    • Coradeschi C 3
    • Tomasini B 3
    (3 authors)
  • 4. Pediatria, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy.
      Authors
    • Grosso S 4
    (1 author)
  • 5. Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Tuscany, Italy.
      Authors
    • Fabbiani A 1, 5
    • Bruttini M 1, 5
    • Mencarelli MA 5
    • Renieri A 1, 5
    • Ariani F 1, 5
    (5 authors)

Frontiers in Genetics, 25 Jan 2023, 14:1143795
https://doi.org/10.3389/fgene.2023.1143795 PMID: 36761000 PMCID: PMC9905838

This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
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This corrects "Spondyloocular Syndrome: A Novel XYLT2 Variant with Description of the Neonatal Phenotype." Front Genet. 2021 Dec 03;12:761264.

Abstract 

[This corrects the article DOI: 10.3389/fgene.2021.761264.].

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Front Genet. 2023; 14: 1143795.
Published online 2023 Jan 25. https://doi.org/10.3389/fgene.2023.1143795
PMCID: PMC9905838
PMID: 36761000

Corrigendum: Spondyloocular syndrome: A novel XYLT2 variant with description of the neonatal phenotype

Gabriella Doddato, 1 , 2 , † Alessandra Fabbiani, 1 , 2 , 3 , † Chiara Fallerini, 1 , 2 Mirella Bruttini, 1 , 2 , 3 Theodora Hadjistilianou, 4 Martino Landi, 5 Caterina Coradeschi, 5 Salvatore Grosso, 6 Barbara Tomasini, 5 Maria Antonietta Mencarelli, 3 Alessandra Renieri, 1 , 2 , 3 and Francesca Arianicorresponding author 1 , 2 , 3 ,*
Author information Article notes Copyright and License information Disclaimer

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.

Articles from Frontiers in Genetics are provided here courtesy of Frontiers Media SA

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Read article at publisher's site: https://doi.org/10.3389/fgene.2023.1143795

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