Patients with SERPINC1 rs2227589 polymorphism found to have multiple cerebral venous sinus thromboses despite a normal antithrombin level: A case report

The hereditary antithrombin (AT) deficiency caused by SERPINC1 gene mutation is an autosomal dominant thrombotic disorder. An increasing number of studies have shown that mutations in the SERPINC1 rs2227589 polymorphic site are correlated with a risk of venous thromboembolism (VTE) at common sites,...

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Veröffentlicht in:	World journal of clinical cases 2022-01, Vol.10 (2), p.618-624
Hauptverfasser:	Liao, Feng, Zeng, Jun-Ling, Pan, Jian-Gang, Ma, Jing, Zhang, Zhi-Jian, Lin, Zhi-Jun, Lin, Li-Feng, Chen, Yu-Sen, Ma, Xiao-Tang
Format:	Artikel
Sprache:	eng
Schlagworte:	Case Report
Online-Zugang:	Volltext
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