论文信息 - The K666N mutation in SF3B1 is associated with increased progression of MDS and distinct RNA splicing. - 字舞流文

The K666N mutation in SF3B1 is associated with increased progression of MDS and distinct RNA splicing.

L. Gondek | Bing Li | B. Smith | M. Levis | I. Gojo | C. Gocke | A. DeZern | Zhijian Xiao | W. B. Dalton | G. Ghiaur | L. Pieterse | J. Donaldson | Eric Helmenstine | W. Dalton