A novel inherited mutation of the transcription factor RUNX1 causes thrombocytopenia and may predispose to acute myeloid leukaemia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2002.03512.x/fullpdf
Reference11 articles.
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2. Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias;Fischer;Blood,1997
3. Linkage of a familial platelet disorder with a propensity to develop myeloid malignancies to human chromosome 21q22.1-22.2;Ho;Blood,1996
4. Dimerization with PEBP2beta protects RUNX1/AML1 from ubiquitin-proteasome-mediated degradation;Huang;EMBO Journal,2001
5. Mutations of the AML1 gene in myelodysplastic syndrome and their functional implications in leukemogenesis;Imai;Blood,2000
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