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Exome sequencing contributes to identify comorbidities in a rare case of infant ARDS induced by the CD40LG mutation

Overview of attention for article published in BMC Medical Genomics, July 2022
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Title
Exome sequencing contributes to identify comorbidities in a rare case of infant ARDS induced by the CD40LG mutation
Published in
BMC Medical Genomics, July 2022
DOI 10.1186/s12920-022-01303-y
Pubmed ID
Authors

Xue Gong, Yunru He, Guoyan Lu, Yulin Zhang, Yu Qiu, Lina Qiao, Yifei Li

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 19 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 19 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 21%
Student > Bachelor 3 16%
Lecturer 1 5%
Student > Doctoral Student 1 5%
Student > Master 1 5%
Other 1 5%
Unknown 8 42%
Readers by discipline Count As %
Social Sciences 2 11%
Neuroscience 2 11%
Agricultural and Biological Sciences 2 11%
Environmental Science 1 5%
Biochemistry, Genetics and Molecular Biology 1 5%
Other 2 11%
Unknown 9 47%