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

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Bibliographic Details
Published in:	Blood
Main Authors:	Tummala, Hemanth, Collopy, Laura C., Walne, Amanda J., Ellison, Alicia, Cardoso, Shirleny, Aksu, Tekin, Yarali, Nese, Aslan, Deniz, Fikret Akata, Rüştü, Teo, Juliana, Songyang, Zhou, Pontikos, Nikolas, Fitzgibbon, Jude, Tomita, Kazunori, Vulliamy, Tom, Dokal, Inderjeet
Format:	Artigo
Language:	Inglês
Published:	American Society of Hematology 2018
Subjects:	Letter to Blood
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC6293869/ https://ncbi.nlm.nih.gov/pubmed/30064976 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2018-03-837799
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