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

The K666N mutation of SF3B1 has distinct clinicopathologic features in MDS. The K666N mutation of SF3B1 has a distinct RNA splicing profile.

Guardat en:
Dades bibliogràfiques
Publicat a:Blood Adv
Autors principals: Dalton, W. Brian, Helmenstine, Eric, Pieterse, Lisa, Li, Bing, Gocke, Christopher D., Donaldson, Joshua, Xiao, Zhijian, Gondek, Lukasz P., Ghiaur, Gabriel, Gojo, Ivana, Smith, B. Douglas, Levis, Mark J., DeZern, Amy E.
Format: Artigo
Idioma:Inglês
Publicat: American Society of Hematology 2020
Matèries:
Stimulus Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7160262/
https://ncbi.nlm.nih.gov/pubmed/32211880
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/bloodadvances.2019001127
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars