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Orphanet Journal of Rare Diseases logoLink to Orphanet Journal of Rare Diseases
. 2021 Jul 19;16:321. doi: 10.1186/s13023-021-01946-7

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

Shengcai Wang 1,#, Wei Wang 2,#, Xuexi Zhang 1,#, Jingang Gui 2, Jie Zhang 1, Yongli Guo 3, Yuanhu Liu 1, Lin Han 4, Qiaoyin Liu 1, Yanzhen Li 1, Nian Sun 1, Zhiyong Liu 1, Jiangnan Du 1, Jun Tai 1,, Xin Ni 1,
PMCID: PMC8290575  PMID: 34281585

Correction to: Orphanet Journal of Rare Diseases (2021) 16:208 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.

Footnotes

Publisher's Note

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

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

Contributor Information

Shengcai Wang, Email: wsc820329@163.com.

Wei Wang, Email: wei860729@163.com.

Xuexi Zhang, Email: chickenzhang007@sina.com.

Jun Tai, Email: trenttj@163.com.

Xin Ni, Email: nixin@bch.com.cn.

Reference

  • 1.Wang et al, A somatic mutation in unravels a novel candidate gene for lymphatic malformation, Orphanet J Rare Dis (2021) 16:208. 10.1186/s13023-021-01782-9 [DOI] [PMC free article] [PubMed]

Articles from Orphanet Journal of Rare Diseases are provided here courtesy of BMC

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