Seventeen novel SERPINC1 variants causing hereditary antithrombin deficiency in a Czech population
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference10 articles.
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2. GFHT study group on Genetic Thrombophilia, Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency;Alhenc-Gelas;Thromb. Haemost.,2017
3. Complete nucleotide sequence of the antithrombin gene: evidence for homologous recombination causing thrombophilia;Olds;Biochemistry,1993
4. High levels of latent antithrombin in plasma from patients with antithrombin deficiency;de la Morena-Barrio;Thromb. Haemost.,2017
5. The genetics of antithrombin;Corral;Thromb. Res.,2018
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