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APA Citation
Pagliari, M. T., Baronciani, L., Garcìa Oya, I., Solimando, M., La Marca, S., Cozzi, G., Stufano, F., Canciani, M. T., & Peyvandi, F. (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), 1251–1259. http://access.bl.uk/ark:/81055/vdc_100040668243.0x000001