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Correction to: A somatic mutation in PIK3CD unravels a novel candidate gene for lymphatic malformation

Orphanet Journal of Rare Diseases volume 16, Article number: 321 (2021) Cite this article

The Original Article was published on 08 May 2021

Correction to: Orphanet Journal of Rare Diseases (2021) 16:208 https://doi.org/10.1186/s13023-021-01782-9

Following the publication of the original article [1] it was brought to our attention that the joint first authorship and equal contribution of Shengcai Wang, Wei Wang and Xuexi Zhang, was not indicated in the published article.

The joint first authorship and equal contribution of the three co-authors has now been marked with dagger symbols in the author list and an explanatory footnote at the end of this Correction.

The original article has also been corrected as above.

Reference

  1. Wang et al, A somatic mutation in unravels a novel candidate gene for lymphatic malformation, Orphanet J Rare Dis (2021) 16:208. https://doi.org/10.1186/s13023-021-01782-9

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Author notes

  1. Shengcai Wang, Wei Wang and Xuexi Zhang are joint first authors who contributed equally to this work

Authors and Affiliations

  1. Department of Otolaryngology-Head and Neck Surgery, National Center for Children’s Health, Beijing Children’s Hospital, Capital Medical University, Beijing, 100045, China

    Shengcai Wang, Xuexi Zhang, Jie Zhang, Yuanhu Liu, Qiaoyin Liu, Yanzhen Li, Nian Sun, Zhiyong Liu, Jiangnan Du, Jun Tai & Xin Ni

  2. Laboratory of Tumor Immunology, National Center for Children’s Health, Beijing Pediatric Research Institute, Beijing Children’s Hospital, Capital Medical University, Beijing, 100045, China

    Wei Wang & Jingang Gui

  3. Beijing Key Laboratory for Pediatric Diseases of Otolaryngology, Head and Neck Surgery, National Center for Children’s Health, Beijing Pediatric Research Institute, Beijing Children’s Hospital, Capital Medical University, Beijing, 100045, China

    Yongli Guo

  4. Running-Gene Inc, Health Valley 602, Beijing, China

    Lin Han

Authors
  1. Shengcai Wang
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  2. Wei Wang
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  3. Xuexi Zhang
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  4. Jingang Gui
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  5. Jie Zhang
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  6. Yongli Guo
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  7. Yuanhu Liu
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  8. Lin Han
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  9. Qiaoyin Liu
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  10. Yanzhen Li
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  11. Nian Sun
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  12. Zhiyong Liu
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  13. Jiangnan Du
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  14. Jun Tai
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  15. Xin Ni
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Corresponding authors

Correspondence to Jun Tai or Xin Ni.

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Wang, S., Wang, W., Zhang, X. et al. Correction to: A somatic mutation in PIK3CD unravels a novel candidate gene for lymphatic malformation. Orphanet J Rare Dis 16, 321 (2021). https://doi.org/10.1186/s13023-021-01946-7

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  • DOI: https://doi.org/10.1186/s13023-021-01946-7

Orphanet Journal of Rare Diseases

ISSN: 1750-1172