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New genetic variant in the SERPINC1 gene: hereditary Antithrombin deficiency case report, familial thrombosis and considerations on genetic counseling

Overview of attention for article published in BMC Medical Genomics, April 2020
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Title
New genetic variant in the SERPINC1 gene: hereditary Antithrombin deficiency case report, familial thrombosis and considerations on genetic counseling
Published in
BMC Medical Genomics, April 2020
DOI 10.1186/s12881-020-01001-5
Pubmed ID
Authors

Margarita E. Polyak, Elena V. Zaklyazminskaya

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 %
Student > Bachelor 3 16%
Student > Doctoral Student 2 11%
Researcher 2 11%
Lecturer > Senior Lecturer 1 5%
Student > Ph. D. Student 1 5%
Other 3 16%
Unknown 7 37%
Readers by discipline Count As %
Medicine and Dentistry 3 16%
Biochemistry, Genetics and Molecular Biology 3 16%
Pharmacology, Toxicology and Pharmaceutical Science 1 5%
Social Sciences 1 5%
Nursing and Health Professions 1 5%
Other 0 0%
Unknown 10 53%