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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Detalles Bibliográficos
Autores principales: Manderstedt, Eric, Lind-Halldén, Christina, Lethagen, Stefan, Halldén, Christer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5794141/
https://www.ncbi.nlm.nih.gov/pubmed/29389944
http://dx.doi.org/10.1371/journal.pone.0192024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5794141/
https://www.ncbi.nlm.nih.gov/pubmed/29389944
http://dx.doi.org/10.1371/journal.pone.0192024

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