A genome-wide association study of LCH identifies a variant in SMAD6 associated with susceptibility

被引:18
|
作者
Peckham-Gregory, Erin C. [1 ,2 ]
Chakraborty, Rikhia [1 ,2 ]
Scheurer, Michael E. [1 ,2 ]
Belmont, John W. [3 ,4 ]
Abhyankar, Harshal [1 ]
Sengal, Amel G. [1 ]
Scull, Brooks P. [1 ]
Eckstein, Olive [1 ]
Zinn, Daniel J. [1 ]
Mayer, Louisa [1 ,2 ]
Shih, Albert [1 ]
Merad, Miriam [5 ]
Parsons, D. Williams [1 ,2 ,3 ]
McClain, Kenneth L. [1 ,2 ]
Lupo, Philip J. [1 ,2 ]
Allen, Carl E. [1 ,2 ]
机构
[1] Texas Childrens Hosp, Texas Childrens Canc & Hematol Ctr, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Pediat, Sect Pediat Hematol Oncol, Room ABBR-R516,Mail Stop BCM305, Houston, TX 77030 USA
[3] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[4] Baylor Coll Med, Childrens Nutr Res Ctr, Houston, TX 77030 USA
[5] Icahn Sch Med Mt Sinai, Tisch Canc Inst, New York, NY 10029 USA
基金
美国国家卫生研究院;
关键词
LANGERHANS-CELL HISTIOCYTOSIS; ACUTE LYMPHOBLASTIC-LEUKEMIA; DISEASE; GENES; RISK; POLYMORPHISMS;
D O I
10.1182/blood-2017-08-800565
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:2229 / 2232
页数:4
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