1. 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). Issue 7 (15th July 2013) Authors: Pagliari, M. T.; Baronciani, L.; Garcìa Oya, I.; Solimando, M.; La Marca, S.; Cozzi, G.; Stufano, F.; Canciani, M. T.; Peyvandi, F. Journal: Journal of thrombosis and haemostasis Issue: Volume 11:Issue 7(2013) Page Start: 1251 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗