Erratum: The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes (The Journal of clinical investigation (2017) 127 6 (2206-2221) PII: 96202)

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

doi:10.1172/JCI96202

Erratum: The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes (The Journal of clinical investigation (2017) 127 6 (2206-2221) PII: 96202)

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

Medicine

Research output: Contribution to journal › Comment/debate › peer-review

4 Scopus citations

Original language	English (US)
Pages (from-to)	3557
Number of pages	1
Journal	The Journal of clinical investigation
Volume	127
Issue number	9
DOIs	https://doi.org/10.1172/JCI96202
State	Published - Sep 1 2017

ASJC Scopus subject areas

Medicine(all)

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Yip, B. H., Steeples, V., Repapi, E., Armstrong, R. N., Llorian, M., Roy, S., Shaw, J., Dolatshad, H., Taylor, S., Verma, A., Bartenstein, M., Vyas, P., Cross, N. C., Malcovati, L., Cazzola, M., Hellström-Lindberg, E., Ogawa, S., Smith, C. W., Pellagatti, A., & Boultwood, J. (2017). Erratum: The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes (The Journal of clinical investigation (2017) 127 6 (2206-2221) PII: 96202). The Journal of clinical investigation, 127(9), 3557. https://doi.org/10.1172/JCI96202

Erratum : The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes (The Journal of clinical investigation (2017) 127 6 (2206-2221) PII: 96202). / Yip, Bon Ham; Steeples, Violetta; Repapi, Emmanouela; Armstrong, Richard N.; Llorian, Miriam; Roy, Swagata; Shaw, Jacqueline; Dolatshad, Hamid; Taylor, Stephen; Verma, Amit; Bartenstein, Matthias; Vyas, Paresh; Cross, Nicholas Cp; Malcovati, Luca; Cazzola, Mario; Hellström-Lindberg, Eva; Ogawa, Seishi; Smith, Christopher Wj; Pellagatti, Andrea; Boultwood, Jacqueline.

In: The Journal of clinical investigation, Vol. 127, No. 9, 01.09.2017, p. 3557.

Research output: Contribution to journal › Comment/debate › peer-review

Yip, BH, Steeples, V, Repapi, E, Armstrong, RN, Llorian, M, Roy, S, Shaw, J, Dolatshad, H, Taylor, S, Verma, A, Bartenstein, M, Vyas, P, Cross, NC, Malcovati, L, Cazzola, M, Hellström-Lindberg, E, Ogawa, S, Smith, CW, Pellagatti, A & Boultwood, J 2017, 'Erratum: The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes (The Journal of clinical investigation (2017) 127 6 (2206-2221) PII: 96202)', The Journal of clinical investigation, vol. 127, no. 9, pp. 3557. https://doi.org/10.1172/JCI96202

Yip, Bon Ham ; Steeples, Violetta ; Repapi, Emmanouela ; Armstrong, Richard N. ; Llorian, Miriam ; Roy, Swagata ; Shaw, Jacqueline ; Dolatshad, Hamid ; Taylor, Stephen ; Verma, Amit ; Bartenstein, Matthias ; Vyas, Paresh ; Cross, Nicholas Cp ; Malcovati, Luca ; Cazzola, Mario ; Hellström-Lindberg, Eva ; Ogawa, Seishi ; Smith, Christopher Wj ; Pellagatti, Andrea ; Boultwood, Jacqueline. / Erratum : The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes (The Journal of clinical investigation (2017) 127 6 (2206-2221) PII: 96202). In: The Journal of clinical investigation. 2017 ; Vol. 127, No. 9. pp. 3557.

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AU - Armstrong, Richard N.

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AU - Dolatshad, Hamid

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Erratum: The U2AF1S34F mutation induces lineage-specific splicing alterations in myelodysplastic syndromes (The Journal of clinical investigation (2017) 127 6 (2206-2221) PII: 96202)

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