In rare acute myeloid leukemia patients harboring both RUNX1 and NPM1 mutations, RUNX1 mutations are unusual in structure and present in the germline

被引：8

作者：

Mendler, Jason H. ^{[1
]}

Maharry, Kati ^{[1
,2
]}

Becker, Heiko ^{[1
]}

Eisfeld, Ann-Kathrin ^{[1
]}

Senter, Leigha ^{[1
]}

Mrozek, Krzysztof ^{[1
]}

Kohlschmidt, Jessica ^{[1
,2
]}

Metzeler, Klaus H. ^{[1
]}

Schwind, Sebastian ^{[1
]}

Whitman, Susan P. ^{[1
]}

Khalife, Jihane ^{[1
]}

Caligiuri, Michael A. ^{[1
]}

Klisovic, Rebecca B. ^{[1
]}

Moore, Joseph O. ^{[3
]}

Carter, Thomas H. ^{[4
]}

Marcucci, Guido ^{[1
]}

Bloomfield, Clara D. ^{[1
]}

机构：

[1] Ohio State Univ, Ctr Comprehens Canc, Columbus, OH 43210 USA

[2] Mayo Clin, Alliance Clin Trials Oncol Stat & Data Ctr, Rochester, MN USA

[3] Duke Univ, Med Ctr, Durham, NC USA

[4] Univ Iowa, Iowa City, IA USA

来源：

HAEMATOLOGICA | 2013年 / 98卷 / 08期

关键词：

acute myeloid leukemia; RUNX1; NPM1; mutations; mutational interrelationships; GROUP-B; YOUNGER; CANCER; EXPRESSION; PSC-833; ADULTS; GENE;

D O I：

10.3324/haematol.2013.089904

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：E92 / E94

页数：3

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