Cite
HARVARD Citation
Smith, N. et al. (2018). Identification and characterization of novel mutations implicated in congenital fibrinogen disorders. Research and practice in thrombosis and haemostasis. 2 (4), pp. 800-811. [Online].
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Smith, N. et al. (2018). Identification and characterization of novel mutations implicated in congenital fibrinogen disorders. Research and practice in thrombosis and haemostasis. 2 (4), pp. 800-811. [Online].