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)
- Author(s)
- Patton, WN; Suthers, G; Altree, M; Carnnichael, C; Wilkins, E; Carroll, J; Rawlings, L; Scott, H;
- Details
- Publication Year 2007-11-16,Volume 110,Issue #11,Page 128B-129B
- Journal Title
- BLOOD
- Publication Type
- Journal Article
- Publisher
- AMER SOC HEMATOLOGY
- Terms of Use/Rights Notice
- Refer to copyright notice on published article.
Creation Date: 2007-11-16 12:00:00