A new rare subtype of hereditary thrombophilia named antithrombin resistance. Antithrombin resistance is caused by mutations in the prothrombin gene (F2), located in the antithrombin binding region, which lead to the impaired thrombin inhibition by antithrombin and, therefore, thrombotic disorders due to the antithrombin resistance.. rare hereditary thrombophilia
收藏NIAID Data Ecosystem2026-03-12 收录
下载链接：
https://www.ncbi.nlm.nih.gov/bioproject/PRJEB45990
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to be published
创建时间：
2021-08-29
