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Article

Thrombotic risk according to SERPINC1 genotype in a large cohort of subjects with antithrombin inherited deficiency.

Thrombosis and haemostasis - 2 Jun 2017

Alhenc-Gelas Martine, Plu-Bureau Genevieve, Hugon-Rodin Justine, Picard Véronique, Horellou Marie-Helene

Abstract excerpt

Inherited quantitative (type I) or qualitative (type II) antithrombin deficiency (ATD) due to mutations in the SERPINC1 gene is a well-known risk factor for venous thromboembolism. ATD may also increase risk for arterial thrombosis. Few studies have investigated risk for thrombosis according to mutations. We addressed this topic in a large retrospective cohort study of 540 heterozygous carriers of SERPINC1...

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Source

Identifiers

PMID: 28300866
DOI: 10.1160/TH16-08-0635

Genes

SERPINC1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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