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
- 1 January 2002
- journal article
- case report
- Published by Elsevier in Thrombosis Research
- Vol. 105 (2) , 135-138
- https://doi.org/10.1016/s0049-3848(02)00007-5
Abstract
No abstract availableKeywords
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