Mutations of ASXL1 and TET2 in aplastic anemia
Copyright policy )Mutations of ASXL1 and TET2 in aplastic anemia
Acquired aplastic anemia (AA), characterized by pancytopenia in peripheral blood (PB) and bone marrow (BM) hypoplasia, is a bone marrow failure syndrome. The late evolution to myelodysplastic syndromes (MDS)/acute myeloid leukemia (AML) is the most common clonal complication in refractory patients
- PEKING UNION MEDICAL COLLEGE China (People's Republic of)
- Chinese Academy of Medical Sciences & Peking Union Medical College China (People's Republic of)
- Institute of Hematology & Blood Diseases Hospital China (People's Republic of)
Heterozygote, Karyotype, Anemia, Aplastic, Dioxygenases, DNA-Binding Proteins, Repressor Proteins, Bone Marrow, Proto-Oncogene Proteins, Mutation, Disease Progression, Humans, Diseases of the blood and blood-forming organs, RC633-647.5
Heterozygote, Karyotype, Anemia, Aplastic, Dioxygenases, DNA-Binding Proteins, Repressor Proteins, Bone Marrow, Proto-Oncogene Proteins, Mutation, Disease Progression, Humans, Diseases of the blood and blood-forming organs, RC633-647.5
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