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86623
Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes
Author(s):
Haan, H.G. de; Vlieg, A.V.; Lotta, L.A.; Gorski, M.M.; Bucciarelli, P.; Martinelli, I.; Baglin, T.P.; Peyvandi, F.; Rosendaal, F.R.; INVENT Consortium
Published
2018
Publication type
Article / Letter to editor
deep vein thrombosis
DNA sequencing
genetics
risk factors
single-nucleotide polymorphisms
Date issued
2018-12-31
Language
English
Is part of
Journal of Thrombosis and Haemostasis (2018), Vol. 16, no. 12, p. 2432-2441
hdl
1887/86623
doi
10.1111/jth.14279
URL
https://onlinelibrary.wiley.com/doi/full/10.1111/jth.14279
Persistent identifier url
https://hdl.handle.net/1887/86623
Documents
01 - Haan_et_al-2018-Journal_of_Thrombosis_and_Haemostasis
version: Not Applicable (or Unknown)
Full text at Publisher's site
Open Access