- Open Access
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)
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  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.
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
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
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