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Seventeen novel SERPINC1 variants causing hereditary antithrombin deficiency in a Czech population
Seventeen novel SERPINC1 variants causing hereditary antithrombin deficiency in a Czech population
2020
Dana Provaznikova
M. Matýšková
Irena Capova
Dagmar Grančarová
Eva Drbohlavová
M. Šlechtová
Hrachovinová I
Keywords:
Hereditary Antithrombin Deficiency
Biochemistry
Czech
Population
Medicine
Physiology
Diabetes mellitus
Antithrombin
Immunology
Antithrombin deficiency
Correction
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