Genetics, diagnosis and clinical features of congenital hypodysfibrinogenemia: a systematic literature review and report of a novel mutation
Journal of Thrombosis and Haemostasis2017Vol. 15(5), pp. 876–888
Citations Over TimeTop 10% of 2017 papers
Alessandro Casini, T. Brungs, Cécile Lavenu‐Bombled, R. Vilar, Marguerite Neerman‐Arbez, Philippe de Moerloose
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