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)
Pagliari, M. T., Baronciani, L., Garcìa Oya, I., Solimando, M., La Marca, S., Cozzi, G., Stufano, F., Canciani, M. T., Peyvandi, F.Volume:
11
Language:
english
Journal:
Journal of Thrombosis and Haemostasis
DOI:
10.1111/jth.12280
Date:
July, 2013
File:
PDF, 314 KB
english, 2013