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Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients
von Willebrand factor (VWF) levels in healthy individuals and in patients with type 1 von Willebrand disease (VWD) are influenced by genetic variation in several genes, e.g. VWF, ABO, STXBP5 and CLEC4M. This study aims to screen comprehensively for CLEC4M variants and investigate their association w...
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| Yayımlandı: | PLoS One |
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| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Public Library of Science
2018
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5794141/ https://ncbi.nlm.nih.gov/pubmed/29389944 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0192024 |
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