| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8458057 | Pathology - Research and Practice | 2018 | 7 Pages |
Abstract
We established a rapid, inexpensive, high-throughput and sensitive method to screen SETBP1 mutations. SETBP1 mutations were a rare molecular event in AML and MDS patients.
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Authors
Xin-yu Yao, Jing-dong Zhou, Jing Yang, Wei Zhang, Ji-chun Ma, Xiang-mei Wen, Dong-ming Yao, Zi-jun Xu, De-hong Wu, Pin-fang He, Jun Qian, Jiang Lin,