DOI:
10.1055/s-00034925
Hämostaseologie
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References
Gallinaro L, Sartorello F, Pontara E. , et al.
Combined partial exon skipping and cryptic splice site activation as a new molecular mechanism for recessive type 1 von Willebrand disease.
Thromb Haemost 2006;
96 (06) 711-716
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