Literature DB >> 32151802

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

Dana Provazníková1, Miloslava Matýšková2, Irena Čápová3, Dagmar Grančarová4, Eva Drbohlavová5, Marie Šlechtová2, Ingrid Hrachovinová6.   

Abstract

Entities:  

Keywords:  Antithrombin; Antithrombin deficiency; Coagulation inhibitor; SERPINC1; Thromboembolism

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Year:  2020        PMID： 32151802     DOI： 10.1016/j.thromres.2020.02.025

Source DB:  PubMed          Journal:  Thromb Res        ISSN： 0049-3848            Impact factor:   3.944


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  2 in total

1.  Detection of Unknown and Rare Pathogenic Variants in Antithrombin, Protein C and Protein S Deficiency Using High-Throughput Targeted Sequencing.

Authors:  Petr Vrtel; Ludek Slavik; Radek Vodicka; Julia Stellmachova; Martin Prochazka; Jana Prochazkova; Jana Ulehlova; Peter Rohon; Tomas Simurda; Jan Stasko; Ivana Martinkova; Radek Vrtel
Journal:  Diagnostics (Basel)       Date:  2022-04-23

2.  Prognostic value of thrombin generation parameters in hospitalized COVID-19 patients.

Authors:  María Eugenia de la Morena-Barrio; Carlos Bravo-Pérez; Antonia Miñano; Belén de la Morena-Barrio; María Piedad Fernandez-Perez; Enrique Bernal; José Miguel Gómez-Verdu; María Teresa Herranz; Vicente Vicente; Javier Corral; María Luisa Lozano
Journal:  Sci Rep       Date:  2021-04-08       Impact factor: 4.379
  2 in total

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