Published in
Elsevier, Thrombosis Research: Vascular Obstruction, Hemorrhage and Hemostasis, (193), p. 5-8, 2020
DOI: 10.1016/j.thromres.2020.05.040
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Identification and expression of a novel heterozygous frameshift mutation in FGA accounting for congenital hypofibrinogenemia in carriers of severe hemophilia A
Journal article published in 2020 by
Rui Vilar,
Alessandro Casini,
Alexandra Fournel,
Guillaume Mourey,
Marguerite Neerman-Arbez 
This paper was not found in any repository, but could be made available legally by the author.
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