Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: von Willebrand Disease and STX2[original query] |
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Effect of genetic variation in STXBP5 and STX2 on von Willebrand factor and bleeding phenotype in type 1 von Willebrand disease patients. PloS one 2012 7 (7): 7. van Loon JE, Sanders YV, de Wee EM, Kruip MJ, de Maat MP, Leebeek FW |
Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients. TH open : companion journal to thrombosis and haemostasis 2020 11 4 (4): e322-e331. Manderstedt Eric, Lind-Halldén Christina, Lethagen Stefan, Halldén Christ |
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- Page last updated:Dec 04, 2023
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