Inherited thrombocytopenia with RUNX1 variants: new French cases with point mutations or large deletions and evidence for a defect in dense granules: P-TH-084
Journal article published in 2011 by
T. Lecompte,
Latger-Cannard,
A. Bouquet,
C. Philippe 
,
C. Preudhomme,
P. Jonveaux,
T. Lecompte,
R. Favier
,
C. Preudhomme,
P. Jonveaux,
T. Lecompte,
R. Favier
