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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