Skip to main content
The Journal of Clinical Investigation logoLink to The Journal of Clinical Investigation
. 2017 Sep 1;127(9):3557. doi: 10.1172/JCI96202

The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes

Bon Ham Yip, Violetta Steeples, Emmanouela Repapi, Richard N Armstrong, Miriam Llorian, Swagata Roy, Jacqueline Shaw, Hamid Dolatshad, Stephen Taylor, Amit Verma, Matthias Bartenstein, Paresh Vyas, Nicholas CP Cross, Luca Malcovati, Mario Cazzola, Eva Hellström-Lindberg, Seishi Ogawa, Christopher WJ Smith, Andrea Pellagatti, Jacqueline Boultwood
PMCID: PMC5669537  PMID: 28862641

Original citation: J Clin Invest. 2017;127(6):2206–2221. https://doi.org/10.1172/JCI91363

Citation for this corrigendum: J Clin Invest. 2017;127(9):3557. https://doi.org/10.1172/JCI96202

In Figure 4D, the horizontal axes of the two graphs were labeled incorrectly, and one sentence in the legend for this part was also incorrect. The correct figure part and sentence are below.

graphic file with name jci-127-96202-g001.jpg

Expression of H2AFY isoform 1.1 and the STRAP long isoform in U2AF1S34F and U2AF1WT transduced cells was measured by isoform-specific qRT-PCR relative to the EV control (red bars: erythroid cells; blue bars: granulomonocytic cells).

The authors regret the error.

Version 1. 09/01/2017

Print issue publication

Footnotes


Articles from The Journal of Clinical Investigation are provided here courtesy of American Society for Clinical Investigation

RESOURCES