HIGH-THROUGHPUT SEQUENCING FOR THE IDENTIFICATION OF DIS3 MUTATIONS IN MULTIPLE MYELOMA

被引:0
作者
Barbieri, M. [1 ]
Lionetti, M. [1 ,2 ]
Todoerti, K. [3 ]
Agnelli, L. [1 ,2 ]
Fabris, S. [1 ]
Cifola, I. [4 ]
Pinatel, E. [4 ]
Tonon, G. [5 ]
Segalla, S. [5 ]
Baldini, L. [1 ,2 ]
Neri, A. [1 ,2 ]
机构
[1] Osped Maggiore Policlin, Fdn IRCCS Ca Granda, Hematol Unit, Milan, Italy
[2] Univ Milan, Dept Clin Sci & Community Hlth, Milan, Italy
[3] IRCCS CROB, Referral Canc Ctr Basilicata, Lab Preclin & Translat Res, Rionero In Vulture, PZ, Italy
[4] CNR, Inst Biomed Technol, Milan, Italy
[5] Ist Sci San Raffaele, Div Expt Oncol, Funct Canc Genom Unit, I-20132 Milan, Italy
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
P262
引用
收藏
页码:159 / 159
页数:1
相关论文
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[1]   The molecular spectrum and clinical impact of DIS3 mutations in multiple myeloma [J].
Weissbach, Susann ;
Langer, Christian ;
Puppe, Bernhard ;
Nedeva, Theodora ;
Bach, Elisa ;
Kull, Miriam ;
Bargou, Ralf ;
Einsele, Hermann ;
Rosenwald, Andreas ;
Knop, Stefan ;
Leich, Ellen .
BRITISH JOURNAL OF HAEMATOLOGY, 2015, 169 (01) :57-70