The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes. (2017)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1172/jci91363
PubMed Identifier: 28436936
Publication URI: http://europepmc.org/abstract/MED/28436936
Type: Journal Article/Review
Volume: 127
Parent Publication: The Journal of clinical investigation
Issue: 6
ISSN: 0021-9738