Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/17694
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dc.contributor.authorTummala, H-
dc.contributor.authorCollopy, LC-
dc.contributor.authorWalne, AJ-
dc.contributor.authorEllison, A-
dc.contributor.authorCardoso, S-
dc.contributor.authorAksu, T-
dc.contributor.authorYarali, N-
dc.contributor.authorAslan, D-
dc.contributor.authorAkata, RF-
dc.contributor.authorTeo, J-
dc.contributor.authorSongyang, Z-
dc.contributor.authorPontikos, N-
dc.contributor.authorFitzgibbon, J-
dc.contributor.authorTomita, K-
dc.contributor.authorVulliamy, T-
dc.contributor.authorDokal, I-
dc.date.accessioned2019-03-13T11:39:16Z-
dc.date.available2018-09-20-
dc.date.available2019-03-13T11:39:16Z-
dc.date.issued2018-09-20-
dc.identifier.citationHemanth Tummala, Laura C. Collopy, Amanda J. Walne, Alicia Ellison, Shirleny Cardoso, Tekin Aksu, Nese Yarali, Deniz Aslan, Rüştü Fikret Akata, Juliana Teo, Zhou Songyang, Nikolas Pontikos, Jude Fitzgibbon, Kazunori Tomita, Tom Vulliamy, Inderjeet Dokal; Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita–like phenotypes. Blood 2018; 132 (12): 1349–1353.en_US
dc.identifier.issn0006-4971-
dc.identifier.issnhttp://dx.doi.org/10.1182/blood-2018-03-837799-
dc.identifier.issn1528-0020-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/17694-
dc.format.extent1349 - 1353-
dc.language.isoenen_US
dc.publisherAmerican Society of Hematologyen_US
dc.titleHomozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita–like phenotypesen_US
dc.typeOtheren_US
dc.identifier.doihttp://dx.doi.org/10.1182/blood-2018-03-837799-
dc.relation.isPartOfBlood-
pubs.issue12-
pubs.publication-statusPublished-
pubs.volume132-
dc.identifier.eissn1528-0020-
Appears in Collections:Dept of Life Sciences Embargoed Research Papers

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