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

Overview of attention for article published in Orphanet Journal of Rare Diseases, May 2021
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Title
A somatic mutation in PIK3CD unravels a novel candidate gene for lymphatic malformation
Published in
Orphanet Journal of Rare Diseases, May 2021
DOI 10.1186/s13023-021-01782-9
Pubmed ID
Authors

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

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 10 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 10 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 4 40%
Student > Master 3 30%
Other 1 10%
Student > Ph. D. Student 1 10%
Unknown 1 10%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 30%
Nursing and Health Professions 2 20%
Medicine and Dentistry 2 20%
Engineering 1 10%
Unknown 2 20%