DOI:
10.1055/s-00033990
TH Open
LinksClose Window
References
Johnson B, Lowe GC, Futterer J. , et al; UK GAPP Study Group.
Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects.
Haematologica 2016;
101 (10) 1170-1179
We do not assume any responsibility for the contents of the web pages of other providers.