Seventeen novel SERPINC1 variants causing hereditary antithrombin deficiency in a Czech population
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu dopisy
PubMed
32151802
DOI
10.1016/j.thromres.2020.02.025
PII: S0049-3848(20)30072-4
Knihovny.cz E-zdroje
- Klíčová slova
- Antithrombin, Antithrombin deficiency, Coagulation inhibitor, SERPINC1, Thromboembolism,
- MeSH
- antithrombin III genetika MeSH
- lidé MeSH
- mutace MeSH
- nedostatek antitrombinu III * genetika MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- dopisy MeSH
- Geografické názvy
- Česká republika epidemiologie MeSH
- Názvy látek
- antithrombin III MeSH
- SERPINC1 protein, human MeSH Prohlížeč
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
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