Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene
Author:
Publisher
Springer Science and Business Media LLC
Subject
Biochemistry (medical),Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry
Link
http://link.springer.com/content/pdf/10.1186/s13039-017-0352-2.pdf
Reference23 articles.
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2. Dokal I, Vulliamy T. Inherited aplastic anaemias/bone marrow failure syndromes. Blood Rev. 2008;22:141–53.
3. Shimamura A, Alter B. Patophysiology and management of inherited bone marrow failure syndromes. Blood Rev. 2010;24:101–22.
4. Kojima S, Ohara A, Tsuchida M, Kudoh T, Hanada R, Okimoto Y, et al. Risk factors for evolution of acquired aplastic anemia into myelodysplastic syndrome and acute myeloid leukemia after immunosuppressive therapy in children. Blood. 2002;100:786–90.
5. Marletta C, Valli R, Pressato B, Mare L, Montalbano G, Menna G, et al. Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes. Mol Cytogenet. 2012;5:39.
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