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Q45861284-7F927EDC-C141-4B3E-A672-768E1C0429CE
Q45861284-7F927EDC-C141-4B3E-A672-768E1C0429CE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45861284-7F927EDC-C141-4B3E-A672-768E1C0429CE
von Willebrand disease type 1 mutation p.Arg1379Cys and the variant p.Ala1377Val synergistically determine a 2M phenotype in four Italian patients.
P2860
Q45861284-7F927EDC-C141-4B3E-A672-768E1C0429CE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45861284-7F927EDC-C141-4B3E-A672-768E1C0429CE
rank
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type
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Statement
wasDerivedFrom
7a5dbcb01c58587a9a3c70dc72e588390fafa5e0
P2860
The type 2B p.R1306W natural mutation of von Willebrand factor dramatically enhances the multimer sensitivity to shear stress.