The common VWF single nucleotide variants c.2365A>G and c.2385T>C modify VWF biosynthesis and clearance

Plasma levels of von Willebrand factor (VWF) vary considerably in the general population and this variation has been linked to several genetic and environmental factors. Genetic factors include 2 common single nucleotide variants (SNVs) located in VWF, rs1063856 (c.2365A>G) and rs1063857 (c.2385T...

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Bibliografische gegevens
Gepubliceerd in:Blood Adv
Hoofdauteurs: Mufti, Ahmad H., Ogiwara, Kenichi, Swystun, Laura L., Eikenboom, Jeroen C. J., Budde, Ulrich, Hopman, Wilma M., Halldén, Christer, Goudemand, Jenny, Peake, Ian R., Goodeve, Anne C., Lillicrap, David, Hampshire, Daniel J.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society of Hematology 2018
Onderwerpen:
Thrombosis and Hemostasis
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6039659/
https://ncbi.nlm.nih.gov/pubmed/29980574
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2017011643
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