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Orphanet Journal of Rare Diseases logoLink to Orphanet Journal of Rare Diseases
. 2025 Sep 25;20:490. doi: 10.1186/s13023-025-04032-4

Correction: Functional characterization of SOX5 variant causing Lamb–Shaffer syndrome and literature review of variants in the SOX5 gene

Ping Wang 1,2, Hanbing Xie 1,2, Xiao Xiao 1,2, He Wang 1,2, Yan Wang 3,✉, Shanling Liu 1,2,✉
PMCID: PMC12465372  PMID: 40999496

Correction: Orphanet Journal of Rare Diseases (2025) 20:300

10.1186/s13023-025-03829-7

Following publication of the original article [1], the authors reported an error in Fig. 1. It was noticed that the figure in the downloadable article PDF unintentionally compromised the anonymity of both individuals.

The correct Fig. 1 is:

graphic file with name 13023_2025_4032_Figa_HTML.jpg

The original article [1] has been updated.

Footnotes

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Contributor Information

Yan Wang, Email: yanwang@swjtu.edu.cn.

Shanling Liu, Email: sunny630@126.com.

References

  • 1.Wang P, Xie H, Xiao X, Wang H, Wang Y, Liu S. Functional characterization of SOX5 variant causing Lamb–Shaffer syndrome and literature review of variants in the SOX5 gene. Orphanet J Rare Dis. 2025;20:300. 10.1186/s13023-025-03829-7. [DOI] [PMC free article] [PubMed] [Google Scholar]

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