Spectrum of abnormalities and clonal transformation in germline RUNX1 familial platelet disorder and a genomic comparative analysis with somatic RUNX1 mutations in MDS/MPN overlap neoplasms

被引：24
|
作者：
DiFilippo, Emma C. [1 ]
Coltro, Giacomo [2 ]
Carr, Ryan M. [2 ]
Mangaonkar, Abhishek A. [2 ]
Binder, Moritz [2 ]
Khan, Shakila P. [3 ]
Rodriguez, Vilmarie [3 ]
Gangat, Naseema [2 ]
Wolanskyj, Alexandra [2 ]
Pruthi, Rajiv K. [2 ]
Chen, Dong [4 ]
He, Rong [4 ]
Viswanatha, David S. [4 ]
Lasho, Terra [2 ]
Finke, Christy [2 ]
Tefferi, Ayalew [2 ]
Pardanani, Animesh [2 ]
Patnaik, Mrinal M. [3 ]
机构：
[1] Mayo Clin, Alix Sch Med, Rochester, MN USA
[2] Mayo Clin, Dept Med, Div Hematol, Rochester, MN USA
[3] Mayo Clin, Div Pediat Hematol, Rochester, MN 55905 USA
[4] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN USA
来源：
LEUKEMIA | 2020年 / 34卷 / 09期
关键词：
ACUTE MYELOID-LEUKEMIA; RISK;
D O I：
10.1038/s41375-020-0752-x
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
引用
收藏
页码：2519 / 2524
页数：6
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