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A large deletion identified in a Swedish family with type 1 VWD.

Thromb Haemost 105(4):733-4 (2011) PMID 21225094

DOI: 10.1160/TH10-08-0556
Version: za2963e q8zaa q8zb5 q8zc3 q8zd0 q8zef q8zfe q8zgd

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