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...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Blood Adv
Main Authors: 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
Idioma:Inglês
Publicado em: American Society of Hematology 2018
Assuntos:
Thrombosis and Hemostasis
Acesso em linha: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
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados