Novel Heritable Mutation of the Transcription Factor RUNX1 as a Cause of Autosomal Dominant Familial Platelet Disorder with Predisposition to Acute Myeloid Leukemia (FPD/AML).

Autor: Patton, William N., Suthers, Graeme *, Altree, Meryl *, Carmichael, Catherine *, Wilkins, Ella *, Carroll, Jacqueline *, Rawlings, Lesley *, Scott, Hamish *
Zdroj: In Blood 16 November 2007 110(11):4244-4244
Databáze: ScienceDirect