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Mutations in inherited fibrinogen disorders correlated with clinical features in the Chinese population.

Journal of thrombosis and thrombolysis - 1 May 2021

Wan Yafang, Li Tian, Zhang Wei, Wang Liying, Zhang Yu, Liao Pu, Liu Shiqiang

Abstract excerpt

Two probands with unknown reasons for low fibrinogen activity were considered to investigate the association between mutations in inherited fibrinogen disorders (IFDs) and clinical features in the Chinese population. A routine coagulation test was conducted on a Sysmex CS5100 coagulation analyzer, and Sanger sequencing was employed to analyze mutations. A PubMed database search through May 2020 was performed to...

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PMID: 32939696
DOI: 10.1007/s11239-020-02283-5

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