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HARVARD Citation
Pagliari, M. et al. (2013). A synonymous (c.3390C>T) or a splice‐site (c.3380‐2A>G) mutation causes exon 26 skipping in four patients with von Willebrand disease (2A/IIE). Journal of thrombosis and haemostasis. 11 (7), pp. 1251-1259. [Online].