A novel family with recessive von Willebrand disease due to compound heterozygosity for a splice site mutation and a missense mutation in the von Willebrand factor gene

Author: Castaman G.   Novella E.   Castiglia E.   Eikenboom J.C.J.   Rodeghiero F.  

Publisher: Elsevier

ISSN: 0049-3848

Source: Thrombosis Research, Vol.105, Iss.2, 2002-01, pp. : 135-138

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