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Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypes

dc.contributor.authorTummala, Hen_US
dc.contributor.authorCollopy, LCen_US
dc.contributor.authorWalne, AJen_US
dc.contributor.authorEllison, Aen_US
dc.contributor.authorCardoso, Sen_US
dc.contributor.authorAksu, Ten_US
dc.contributor.authorYarali, Nen_US
dc.contributor.authorAslan, Den_US
dc.contributor.authorAkata, RFen_US
dc.contributor.authorTeo, Jen_US
dc.contributor.authorSongyang, Zen_US
dc.contributor.authorPontikos, Nen_US
dc.contributor.authorFitzgibbon, Jen_US
dc.contributor.authorTomita, Ken_US
dc.contributor.authorVulliamy, Ten_US
dc.contributor.authorDokal, Ien_US
dc.date.accessioned2018-08-01T09:04:05Z
dc.date.available2018-07-26en_US
dc.date.issued2018-09-20en_US
dc.date.submitted2018-07-27T15:14:50.017Z
dc.identifier.issn0006-4971en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/42823
dc.format.extent1349 - 1353en_US
dc.language.isoenen_US
dc.relation.ispartofBLOODen_US
dc.titleHomozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypesen_US
dc.typeArticle
dc.rights.holder© 2018 American Society of Hematology
dc.identifier.doi10.1182/blood-2018-03-837799en_US
pubs.author-urlhttp://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000445097300015&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=612ae0d773dcbdba3046f6df545e9f6aen_US
pubs.issue12en_US
pubs.notesNo embargoen_US
pubs.publication-statusPublisheden_US
pubs.volume132en_US


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