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Point mutation E1099K in MMSET/NSD2 enhances its methyltranferase activity and leads to altered global chromatin methylation in lymphoid malignancies

dc.contributor.authorOyer, JA
dc.contributor.authorHuang, X
dc.contributor.authorZheng, Y
dc.contributor.authorShim, J
dc.contributor.authorEzponda, T
dc.contributor.authorCarpenter, Z
dc.contributor.authorAllegretta, M
dc.contributor.authorOkot-Kotber, CI
dc.contributor.authorPatel, JP
dc.contributor.authorMelnick, A
dc.contributor.authorLevine, RL
dc.contributor.authorMackerell, AD
dc.contributor.authorKelleher, NL
dc.contributor.authorLicht, JD
dc.contributor.authorPopovic, R
dc.date.accessioned2013-10-28T08:54:04Z
dc.date.available2013-10-28T08:54:04Z
dc.date.issued2013
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/23823660
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/57945
dc.language.isoenen
dc.titlePoint mutation E1099K in MMSET/NSD2 enhances its methyltranferase activity and leads to altered global chromatin methylation in lymphoid malignanciesen
dc.typeArticleen
local.publisherCollege of Biological and Physical Sciences ,Department of physicsen


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