New Search

Advanced search
Export article
Open Access

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

Sciprofile linkW. Brian Dalton, Eric Helmenstine, Lisa Pieterse, Bing Li, Sciprofile linkChristopher D. Gocke, Joshua Donaldson, Zhijian Xiao, Lukasz P. Gondek, Sciprofile linkGabriel Ghiaur, Ivana Gojo, B. Douglas Smith, Sciprofile linkMark Levis, Amy E. DeZern
Published: 14 April 2020
Blood Advances , Volume 4, pp 1192-1196; doi:10.1182/bloodadvances.2019001127

Abstract: The K666N mutation of SF3B1 has distinct clinicopathologic features in MDS. The K666N mutation of SF3B1 has a distinct RNA splicing profile.
Keywords: splicing / MDS / clinicopathologic / K666N mutation of SF3B1 / SF3B1 is associated

Scifeed alert for new publications

Never miss any articles matching your research from any publisher
  • Get alerts for new papers matching your research
  • Find out the new papers from selected authors
  • Updated daily for 49'000+ journals and 6000+ publishers
  • Define your Scifeed now

Share this article

Click here to see the statistics on "Blood Advances" .
References (15)
    Back to Top Top