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Q24300940-6425D6C8-96D5-4272-A8B9-C5FCEEB0A9C3
Q24300940-6425D6C8-96D5-4272-A8B9-C5FCEEB0A9C3
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http://www.wikidata.org/entity/statement/Q24300940-6425D6C8-96D5-4272-A8B9-C5FCEEB0A9C3
Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion
P2860
Q24300940-6425D6C8-96D5-4272-A8B9-C5FCEEB0A9C3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24300940-6425D6C8-96D5-4272-A8B9-C5FCEEB0A9C3
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wasDerivedFrom
132827a8feb9c488000e35f32f76d0a22f03f501
P2860
Expression and characterization of von Willebrand factor dimerization defects in different types of von Willebrand disease.