DOI:
10.1055/s-00033990
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References
Mufti AH, Alyami NH, Peake IR. , et al.
Silent von Willebrand factor variant c.4146G>T (p.Leu1382=) causes type 1 von Willebrand disease via disruption of an exonic splice enhancer motif [abstract].
Res Pract Thromb Haemost 2017;
1 (Suppl. 01) 147-148
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