Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients.

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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Bibliographic Details
Main Authors: Eric Manderstedt, Christina Lind-Halldén, Stefan Lethagen, Christer Halldén
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5794141?pdf=render

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