Correction to: A somatic mutation in\xa0PIK3CD unravels a\xa0novel candidate gene for\xa0lymphatic malformation

Jingang Gui,Xin Ni,Shengcai Wang,Jun Tai,Zhiyong Liu,Lin Han,Jie Zhang,Yanzhen Li,Yuanhu Liu,Wei Wang,Nian Sun,Yongli Guo,Jiangnan Du,Qiaoyin Liu,Xuexi Zhang

doi:10.1186/s13023-021-01946-7

Abstract

Correction to: A somatic mutation in\xa0PIK3CD unravels a\xa0novel candidate gene for\xa0lymphatic malformation

Highlights

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 been marked with dagger symbols in the author list and an explanatory footnote at the end of this Correction
*Correspondence: trenttj@163.com; nixin@bch.com.cn †Shengcai Wang, Wei Wang and Xuexi Zhang are joint first authors who contributed to this work 1 Department of Otolaryngology‐Head and Neck Surgery, National Center for Children’s Health, Beijing Children’s Hospital, Capital Medical University, Beijing 100045, China Full list of author information is available at the end of the article

Summary

Introduction

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. Correction to: A somatic mutation in PIK3CD unravels a novel candidate gene for lymphatic malformation Shengcai Wang1†, Wei Wang2†, Xuexi Zhang1†, Jingang Gui2, Jie Zhang1, Yongli Guo3, Yuanhu Liu1, Lin Han4, Qiaoyin Liu1, Yanzhen Li1, Nian Sun1, Zhiyong Liu1, Jiangnan Du1, Jun Tai1* and Xin Ni1*

Results

Conclusion