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 * |
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Zdroj: | In Blood 16 November 2007 110(11):4244-4244 |
Databáze: | ScienceDirect |
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