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Article

Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A.

Thrombosis research - 1 Sept 2020

Vilar Rui, Casini Alessandro, Fournel Alexandra, Mourey Guillaume, Neerman-Arbez Marguerite

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Identifiers

PMID: 32497950
DOI: 10.1016/j.thromres.2020.05.040

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