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A novel TAB2 nonsense mutation (p.S149X) causing autosomal dominant congenital heart defects: a case report of a Chinese family

Overview of attention for article published in BMC Cardiovascular Disorders, January 2020
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Title
A novel TAB2 nonsense mutation (p.S149X) causing autosomal dominant congenital heart defects: a case report of a Chinese family
Published in
BMC Cardiovascular Disorders, January 2020
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

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%