Please use this identifier to cite or link to this item:
http://bura.brunel.ac.uk/handle/2438/17694
Title: | Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita–like phenotypes |
Authors: | Tummala, H Collopy, LC Walne, AJ Ellison, A Cardoso, S Aksu, T Yarali, N Aslan, D Akata, RF Teo, J Songyang, Z Pontikos, N Fitzgibbon, J Tomita, K Vulliamy, T Dokal, I |
Issue Date: | 20-Sep-2018 |
Publisher: | American Society of Hematology |
Citation: | Hemanth 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. |
URI: | http://bura.brunel.ac.uk/handle/2438/17694 |
DOI: | http://dx.doi.org/10.1182/blood-2018-03-837799 |
ISSN: | 0006-4971 http://dx.doi.org/10.1182/blood-2018-03-837799 1528-0020 |
Appears in Collections: | Dept of Life Sciences Embargoed Research Papers |
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FullText.pdf | 1.29 MB | Adobe PDF | View/Open |
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