DOI:
10.1055/s-00034925
Hämostaseologie
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References
Fan J, Ling J, Zhou H, He J, Hu S.
Case report: an infant with severe thrombocytopenia diagnosed with type 2B von Willebrand disease due to a de novo p.Val1316Met mutation.
Turk J Haematol 2020;
37 (04) 296-298
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