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A novel PIK3R1 mutation of SHORT syndrome in a Chinese female with diffuse thyroid disease: a case report and review of literature

Overview of attention for article published in BMC Medical Genomics, October 2020
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Citations

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Title
A novel PIK3R1 mutation of SHORT syndrome in a Chinese female with diffuse thyroid disease: a case report and review of literature
Published in
BMC Medical Genomics, October 2020
DOI 10.1186/s12881-020-01146-3
Pubmed ID
Authors

Liying Sun, Qianwen Zhang, Qun Li, Yijun Tang, Yirou Wang, Xin Li, Niu Li, Jian Wang, Xiumin Wang

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 %
Unspecified 3 16%
Student > Bachelor 2 11%
Student > Doctoral Student 2 11%
Student > Master 2 11%
Student > Ph. D. Student 1 5%
Other 1 5%
Unknown 8 42%
Readers by discipline Count As %
Medicine and Dentistry 5 26%
Unspecified 3 16%
Biochemistry, Genetics and Molecular Biology 1 5%
Psychology 1 5%
Nursing and Health Professions 1 5%
Other 0 0%
Unknown 8 42%