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TH13-06-0462
TH13-06-0462
http://dx.doi.org/10.1160/TH13-06-0462
Characterisation of the p.A1461D mutation causing von Willebrand disease type 2B with severe thrombocytopenia, circulating giant platelets, and defective α-granule secretion.
P356
Q54441484-7E0DFE89-16B0-49BA-8904-FD27E4D991FB
P356
TH13-06-0462
http://dx.doi.org/10.1160/TH13-06-0462