DOI:
10.1055/s-00035024
Thrombosis and Haemostasis
LinksClose Window
References
Pintao MC, Garcia AA, Borgel D. , et al.
Gross deletions/duplications in PROS1 are relatively common in point mutation-negative hereditary protein S deficiency.
Hum Genet 2009;
126 (03) 449-456
We do not assume any responsibility for the contents of the web pages of other providers.