Next‐generation sequencing study finds an excess of rare, coding single‐nucleotide variants of ADAMTS13 in patients with deep vein thrombosis
Luca A. Lotta, Giacomo Tuana, Jin Yu, Ida Martinelli, M. Wang, Fei Yu, Serena M. Passamonti, Emanuela Pappalardo, Carla Valsecchi, Steven E. Scherer, Walker Hale, Donna M. Muzny, G. Randi, Frits R. Rosendaal, Richard A. Gibbs, Flora Peyvandi (2013). Next‐generation sequencing study finds an excess of rare, coding single‐nucleotide variants of ADAMTS13 in patients with deep vein thrombosis. Journal of Thrombosis and Haemostasis, 11(7), pp. 1228-1239, DOI: 10.1111/jth.12291.
