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Genome-wide studies of von Willebrand Factor Propeptide Identify Loci Contributing to Variation in Propeptide Levels and von Willebrand Factor Clearance
BACKGROUND: Previous studies identified common variants at the ABO and VWF loci and unknown variants in a chromosome 2q12 linkage interval that contributed to the variation of plasma von Willebrand factor levels (VWF). While the association with ABO haplotypes can be explained by differential VWF cl...
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| Publicat a: | J Thromb Haemost |
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| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5035595/ https://ncbi.nlm.nih.gov/pubmed/27359253 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jth.13401 |
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