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Genotype-phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryo.

British journal of haematology - 1 Oct 2020

Bravo-Pérez C, de la Morena-Barrio M E, Palomo A, Entrena L, de la Morena-Barrio B, Padilla J, Miñano A, Navarro E, Cifuentes R, Corral J, Vicente V

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Share to Antithrombin III
Share to Antithrombin III Deficiency
Share to Blood Coagulation and Thrombosis Mechanisms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 32686144
DOI: 10.1111/bjh.16963

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Genotype-phenotype gradient of SERPINC1 variants in a single family reveals a severe compound antithrombin deficiency in a dead embryo.PMID 32686144Read ↗

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