Clinical and molecular features of acute promyelocytic leukemia with variant retinoid acid receptor fusions

Clinical and molecular features of acute promyelocytic leukemia with variant retinoid acid receptor fusions
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具有变异视黄酸受体融合的急性早幼粒细胞白血病的临床和分子特征

DOI:
10.3324/haematol.2018.205369
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发表时间:
2018-09
期刊:
Haematologica-The Hematology Journal
影响因子:
--
通讯作者:
Chen Suning
Chen Suning
中科院分区:
其他
文献类型:
--
作者:
Wen Lijun;Xu Yang;Yao Li;Wang Nana;Wang Qinrong;Liu Tianhui;Pan Jinlan;Cen Jiannong;Zhou Huifeng;Miao Miao;Shao Yang W;Wang Xiaonan;Wang Xiaoxia;Ruan Changgeng;Wu Depei;Chen Suning

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急性早幼粒细胞白血病(APL)是急性髓细胞白血病(AML)中的一种独特疾病,其特征是早幼粒细胞期白血病细胞块的扩增。绝大多数APL患者的染色体上携带t(15;17)(q24;q21),涉及早幼粒细胞白血病(PML)基因
Acute promyelocytic leukemia (APL) is a unique disease entity in acute myeloid leukemia (AML), characterized by the expansion of leukemic cell block at the promyelocytic stage. The vast majority of APL patients bear t(15;17)(q24;q21) involving the promyelocytic leukemia ( PML ) gene at chromosome
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