Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: von Willebrand Disease and STXBP5[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 |
Genome-wide association studies identify genetic loci for low von Willebrand factor levels.
![]() European journal of human genetics : EJHG 2015 Oct . van Loon Janine, Dehghan Abbas, Weihong Tang, Trompet Stella, McArdle Wendy L, Asselbergs Folkert F W, Chen Ming-Huei, Lopez Lorna M, Huffman Jennifer E, Leebeek Frank W G, Basu Saonli, Stott David J, Rumley Ann, Gansevoort Ron T, Davies Gail, Wilson James J F, Witteman Jacqueline C M, Cao Xiting, de Craen Anton J M, Bakker Stephan J L, Psaty Bruce M, Starr John M, Hofman Albert, Wouter Jukema J, Deary Ian J, Hayward Caroline, van der Harst Pim, Lowe Gordon D O, Folsom Aaron R, Strachan David P, Smith Nicolas, de Maat Moniek P M, O'Donnell Christoph |
Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients. Thrombosis and haemostasis 2018 Jul . Lind-Halldén Christina, Manderstedt Eric, Carlberg Daniel, Lethagen Stefan, Halldén Christ |
Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients. PloS one 2018 13 (2): e0192024. Manderstedt Eric, Lind-Halldén Christina, Lethagen Stefan, Halldén Christ |
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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