Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: von Willebrand Disease and CLEC4M[original query] |
---|
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 |
- Page last reviewed:Feb 1, 2024
- Content source: