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A novel von Willebrand factor mutation (11372S) associated with type 2B-like von Willebrand disease : An elusive phenotype and a difficult diagnosisCASONATO, Alessandra; SARTORELLO, Francesca; PONTARA, Elena et al.Thrombosis and haemostasis. 2007, Vol 98, Num 6, pp 1182-1187, issn 0340-6245, 6 p.Article

Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type I von Willebrand diseaseGALLINARO, Lisa; SARTORELLO, Francesca; PONTARA, Elena et al.Thrombosis and haemostasis. 2006, Vol 96, Num 6, pp 711-716, issn 0340-6245, 6 p.Article

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