Next-generation sequencing study finds an excess of rare, coding single-nucleotide variants of ADAMTS13 in patients with deep vein thrombosis

Author(s):
Lotta, L.A.; Tuana, G.; Yu, J.; Martinelli, I.; Wang, M.; Yu, F.; Passamonti, S.M.; Pappalardo, E.; Valsecchi, C.; Scherer, S.E.; Hale, W.; Muzny, D.M.; Randi, G.; Rosendaal, F.R.; Gibbs, R.A.; Peyvandi, F.
Published
2013
Publication type
Article / Letter to editor
ADAMTS-13deep vein thrombosisexomevenous thromboembolismVWF
Date issued
2013-07-31
Language
English
Is part of
Journal of Thrombosis and Haemostasis (2013), Vol. 11, no. 7, p. 1228-1239
hdl
1887/99839
doi
10.1111/jth.12291