DOI:
10.1055/s-00033990
TH Open
LinksClose Window
References
Leo VC, Morgan NV, Bem D. , et al; UK GAPP Study Group.
Use of next-generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders.
J Thromb Haemost 2015;
13 (04) 643-650
We do not assume any responsibility for the contents of the web pages of other providers.