Please use this identifier to cite or link to this item: https://doi.org/10.1038/ncomms7042
DC FieldValue
dc.titleAberrant splicing of U12-type introns is the hallmark of ZRSR2 mutant myelodysplastic syndrome
dc.contributor.authorMadan V.
dc.contributor.authorKanojia D.
dc.contributor.authorLi J.
dc.contributor.authorOkamoto R.
dc.contributor.authorSato-Otsubo A.
dc.contributor.authorKohlmann A.
dc.contributor.authorSanada M.
dc.contributor.authorGrossmann V.
dc.contributor.authorSundaresan J.
dc.contributor.authorShiraishi Y.
dc.contributor.authorMiyano S.
dc.contributor.authorThol F.
dc.contributor.authorGanser A.
dc.contributor.authorYang H.
dc.contributor.authorHaferlach T.
dc.contributor.authorOgawa S.
dc.contributor.authorKoeffler H.P.
dc.date.accessioned2016-09-20T01:42:38Z
dc.date.available2016-09-20T01:42:38Z
dc.date.issued2015
dc.identifier.citationMadan V., Kanojia D., Li J., Okamoto R., Sato-Otsubo A., Kohlmann A., Sanada M., Grossmann V., Sundaresan J., Shiraishi Y., Miyano S., Thol F., Ganser A., Yang H., Haferlach T., Ogawa S., Koeffler H.P. (2015). Aberrant splicing of U12-type introns is the hallmark of ZRSR2 mutant myelodysplastic syndrome. Nature Communications 6. ScholarBank@NUS Repository. https://doi.org/10.1038/ncomms7042
dc.identifier.issn20411723
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/127877
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1038/ncomms7042
dc.publisherNature Publishing Group
dc.typeArticle
dc.contributor.departmentMEDICINE
dc.description.doi10.1038/ncomms7042
dc.description.sourcetitleNature Communications
dc.description.volume6
dc.identifier.isiut000348830000004
dc.published.statepublished
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

SCOPUSTM   
Citations

134
checked on Jun 21, 2022

WEB OF SCIENCETM
Citations

128
checked on Jun 21, 2022

Page view(s)

142
checked on Jun 23, 2022

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.