Show simple item record

Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia

dc.contributor.authorCardoso, SRen_US
dc.contributor.authorRyan, Gen_US
dc.contributor.authorWalne, AJen_US
dc.contributor.authorEllison, Aen_US
dc.contributor.authorLowe, Ren_US
dc.contributor.authorTummala, Hen_US
dc.contributor.authorRio-Machin, Aen_US
dc.contributor.authorCollopy, Len_US
dc.contributor.authorAl Seraihi, Aen_US
dc.contributor.authorWallis, Yen_US
dc.contributor.authorPage, Pen_US
dc.contributor.authorAkiki, Sen_US
dc.contributor.authorFitzgibbon, Jen_US
dc.contributor.authorVulliamy, Ten_US
dc.contributor.authorDokal, Ien_US
dc.date.accessioned2016-05-09T12:42:10Z
dc.date.available2016-04-13en_US
dc.date.issued2016-10en_US
dc.date.submitted2016-05-04T10:39:41.570Z
dc.identifier.issn0887-6924en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/12225
dc.description.sponsorshipThe Brazilian National Council for Scientific and Technological Development), Bloodwise, Children with Cancer and MRC (Medical Research Council, UK).en_US
dc.format.extent2083 - 2086en_US
dc.language.isoenen_US
dc.relation.ispartofLEUKEMIAen_US
dc.rightsThis work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permissionfrom the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
dc.titleGermline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemiaen_US
dc.typeArticle
dc.rights.holder© 2016 Macmillan Publishers Limited, part of Springer Nature.
dc.identifier.doi10.1038/leu.2016.124en_US
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000385801500018&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue10en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume30en_US
qmul.funderThe genetic basis and pathophysiology of dyskeratosis congenita, aplastic anaemia, myelodysplasia and related disorders::Wellcome Trusten_US
qmul.funderThe genetic basis and pathophysiology of dyskeratosis congenita, aplastic anaemia, myelodysplasia and related disorders::Wellcome Trusten_US
qmul.funderThe genetic basis and pathophysiology of dyskeratosis congenita, aplastic anaemia, myelodysplasia and related disorders::Wellcome Trusten_US


Files in this item

Thumbnail
Name:
Dokal Germline heterozygous DDX41 ...
Size:
597.9Kb
Format:
application/
Description:
Published version
View/Open

This item appears in the following Collection(s)

Show simple item record