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Role of PUF60 gene in Verheij syndrome: a case report of the first Chinese Han patient with a de novo pathogenic variant and review of the literature

Overview of attention for article published in BMC Medical Genomics, October 2018
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Title
Role of PUF60 gene in Verheij syndrome: a case report of the first Chinese Han patient with a de novo pathogenic variant and review of the literature
Published in
BMC Medical Genomics, October 2018
DOI 10.1186/s12920-018-0421-3
Pubmed ID
Authors

Qiong Xu, Chun-yang Li, Yi Wang, Hui-ping Li, Bing-bing Wu, Yong-hui Jiang, Xiu Xu

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 20 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 20 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 4 20%
Other 3 15%
Student > Doctoral Student 3 15%
Student > Master 3 15%
Student > Bachelor 2 10%
Other 3 15%
Unknown 2 10%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 7 35%
Medicine and Dentistry 5 25%
Agricultural and Biological Sciences 2 10%
Unspecified 1 5%
Sports and Recreations 1 5%
Other 1 5%
Unknown 3 15%