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Mendeley readers
Title |
A novel TAB2 nonsense mutation (p.S149X) causing autosomal dominant congenital heart defects: a case report of a Chinese family
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Published in |
BMC Cardiovascular Disorders, January 2020
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DOI | 10.1186/s12872-019-01322-1 |
Pubmed ID | |
Authors |
Jia Chen, Huizhen Yuan, Kang Xie, Xinrong Wang, Linglong Tan, Yongyi Zou, Yan Yang, Lu Pan, Junfang Xiao, Ge Chen, Yanqiu Liu |
Mendeley readers
The data shown below were compiled from readership statistics for 37 Mendeley readers of this research output. Click here to see the associated Mendeley record.
Geographical breakdown
Country | Count | As % |
---|---|---|
Unknown | 37 | 100% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Ph. D. Student | 6 | 16% |
Student > Bachelor | 4 | 11% |
Student > Master | 3 | 8% |
Researcher | 3 | 8% |
Unspecified | 1 | 3% |
Other | 3 | 8% |
Unknown | 17 | 46% |
Readers by discipline | Count | As % |
---|---|---|
Medicine and Dentistry | 12 | 32% |
Agricultural and Biological Sciences | 2 | 5% |
Unspecified | 1 | 3% |
Biochemistry, Genetics and Molecular Biology | 1 | 3% |
Nursing and Health Professions | 1 | 3% |
Other | 2 | 5% |
Unknown | 18 | 49% |