Seventeen novel SERPINC1 variants causing hereditary antithrombin deficiency in a Czech population
Language English Country United States Media print-electronic
Document type Letter
PubMed
32151802
DOI
10.1016/j.thromres.2020.02.025
PII: S0049-3848(20)30072-4
Knihovny.cz E-resources
- Keywords
- Antithrombin, Antithrombin deficiency, Coagulation inhibitor, SERPINC1, Thromboembolism,
- MeSH
- Antithrombin III genetics MeSH
- Humans MeSH
- Mutation MeSH
- Antithrombin III Deficiency * genetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Letter MeSH
- Geographicals
- Czech Republic epidemiology MeSH
- Names of Substances
- Antithrombin III MeSH
- SERPINC1 protein, human MeSH Browser
Clinical Biochemistry and Hematology Department Hospital Karlovy Vary Karlovy Vary Czech Republic
Clinical Hematology Department Hospital Liberec Liberec Czech Republic
Clinical Hematology Department University Hospital Brno Brno Czech Republic
NRL for Disorders in Hemostasis Institute of Hematology and Blood Transfusion Prague Czech Republic
Thrombosis and Hemostasis Center Institute of Hematology and Blood Transfusion Prague Czech Republic
References provided by Crossref.org
