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Q30411744-056BD9C3-347C-487E-8D01-10A0DF97E199
Q30411744-056BD9C3-347C-487E-8D01-10A0DF97E199
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30411744-056BD9C3-347C-487E-8D01-10A0DF97E199
Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project.
P2860
Q30411744-056BD9C3-347C-487E-8D01-10A0DF97E199
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30411744-056BD9C3-347C-487E-8D01-10A0DF97E199
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wasDerivedFrom
30aee06adb81fcac77c93443edc891aff78fe0e4
P2860
The defective interaction between von Willebrand factor and factor VIII in a patient with type 1 von Willebrand disease is caused by substitution of Arg19 and His54 in mature von Willebrand factor.