Seventeen novel SERPINC1 variants causing hereditary...

Thrombosis Research 2020 / 05 Vol. 189

Seventeen novel SERPINC1 variants causing hereditary antithrombin deficiency in a Czech population

Provazníková, Dana, Matýšková, Miloslava, Čápová, Irena, Grančarová, Dagmar, Drbohlavová, Eva, Šlechtová, Marie, Hrachovinová, Ingrid
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Volume:
189
Language:
english
Journal:
Thrombosis Research
DOI:
10.1016/j.thromres.2020.02.025
Date:
May, 2020
File:
PDF, 621 KB
english, 2020
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