Novel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome

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dc.contributor.authorJongmans, M.
dc.contributor.authorKuiper, R.
dc.contributor.authorCarmichael, C.
dc.contributor.authorWilkins, E.
dc.contributor.authorDors, N.
dc.contributor.authorCarmagnac, A.
dc.contributor.authorSchouten-van Meeteren, N.
dc.contributor.authorLi, X.
dc.contributor.authorStankovic, M.
dc.contributor.authorKamping, E.
dc.contributor.authorBengtsson, H.
dc.contributor.authorSchoenmakers, M.
dc.contributor.authorGeurts van Kessel, A.
dc.contributor.authorHoogerbrugge, P.
dc.contributor.authorHahn, C.
dc.contributor.authorBrons, P.
dc.contributor.authorScott, H.
dc.contributor.authorHoogerbrugge, N.
dc.date.issued2010
dc.description.statementofresponsibilityMCJ Jongmans, RP Kuiper, CL Carmichael, EJ Wilkins, N Dors, A Carmagnac, AYN Schouten-van Meeteren, X Li, M Stankovic, E Kamping, H Bengtsson, EFPM Schoenmakers, A Geurts van Kessel, PM Hoogerbrugge, CN Hahn, PP Brons, HS Scott and N Hoogerbrugge
dc.identifier.citationLeukemia, 2010; 24(1):242-246
dc.identifier.doi10.1038/leu.2009.210
dc.identifier.issn0887-6924
dc.identifier.issn1476-5551
dc.identifier.orcidHahn, C. [0000-0001-5105-2554]
dc.identifier.orcidScott, H. [0000-0002-5813-631X]
dc.identifier.urihttp://hdl.handle.net/2440/62193
dc.language.isoen
dc.publisherNature Publishing Group
dc.rights© 2010 Nature Publishing Group
dc.source.urihttps://doi.org/10.1038/leu.2009.210
dc.subjectHumans
dc.subjectBlood Platelet Disorders
dc.subjectGene Deletion
dc.subjectMutation
dc.subjectChild
dc.subjectChild, Preschool
dc.subjectFemale
dc.subjectMale
dc.subjectCore Binding Factor Alpha 2 Subunit
dc.subjectLeukemia, Myeloid, Acute
dc.titleNovel RUNX1 mutations in familial platelet disorder with enhanced risk for acute myeloid leukemia: clues for improved identification of the FPD/AML syndrome
dc.typeJournal article
pubs.publication-statusPublished

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