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Q45861284-7F1EB449-B3A1-4207-9752-959C3432971B
Q45861284-7F1EB449-B3A1-4207-9752-959C3432971B
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Statement
http://www.wikidata.org/entity/statement/Q45861284-7F1EB449-B3A1-4207-9752-959C3432971B
von Willebrand disease type 1 mutation p.Arg1379Cys and the variant p.Ala1377Val synergistically determine a 2M phenotype in four Italian patients.
P2860
Q45861284-7F1EB449-B3A1-4207-9752-959C3432971B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45861284-7F1EB449-B3A1-4207-9752-959C3432971B
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type
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wasDerivedFrom
7a5dbcb01c58587a9a3c70dc72e588390fafa5e0
P2860
Evaluation of an heterogeneous group of patients with von Willebrand disease using an assay alternative to ristocetin induced platelet agglutination.