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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Publicado en:Blood Adv
Autores principales: 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.
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society of Hematology 2018
Materias:
Thrombosis and Hemostasis
Acceso en línea: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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