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ERRATUM article

Front. Genet., 25 January 2024
Sec. Genetics of Common and Rare Diseases
Volume 15 - 2024 | https://doi.org/10.3389/fgene.2024.1372019

Erratum: Case report: atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum

This article is an erratum on:

  1. Case report: atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum

    1. Read original article
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An Erratum on
Case report: atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum

by Vimercati A, Tannorella P, Orlandini E, Calzari L, Moro M, Guzzetti S, Selicorni A, Crippa M, Larizza L, Bonati MT and Russo S (2023). Front. Genet. 14:1198821. doi: 10.3389/fgene.2023.1198821

Due to a production error, the title of the original article was incorrectly modified, using “Case report: a typical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum” instead of “Case report: atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum”.

The publisher apologizes for this mistake. The original version of this article has been updated.

Publisher’s note

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: Silver-Russell syndrome, unexpected molecular results, body asymmetry, IGF2, hand dystonia, VPS16, endolysosomal pathway

Citation: Frontiers Production Office (2024) Erratum: Case report: atypical Silver-Russell syndrome patient with hand dystonia: the valuable support of the consensus statement to the wide syndromic spectrum. Front. Genet. 15:1372019. doi: 10.3389/fgene.2024.1372019

Received: 17 January 2024; Accepted: 17 January 2024;
Published: 25 January 2024.

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Frontiers Editorial Office, Frontiers Media SA, Switzerland

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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.