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A novel deletion variant in TRAPPC2 causes spondyloepiphyseal dysplasia tarda in a five-generation Chinese family

Overview of attention for article published in BMC Medical Genomics, May 2020
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Title
A novel deletion variant in TRAPPC2 causes spondyloepiphyseal dysplasia tarda in a five-generation Chinese family
Published in
BMC Medical Genomics, May 2020
DOI 10.1186/s12881-020-01052-8
Pubmed ID
Authors

Cai Zhang, Caiqi Du, Juan Ye, Feng Ye, Renfa Wang, Xiaoping Luo, Yan Liang

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 16 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 16 100%

Demographic breakdown

Readers by professional status Count As %
Student > Postgraduate 2 13%
Student > Ph. D. Student 1 6%
Researcher 1 6%
Student > Doctoral Student 1 6%
Unknown 11 69%
Readers by discipline Count As %
Medicine and Dentistry 3 19%
Biochemistry, Genetics and Molecular Biology 2 13%
Unknown 11 69%