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

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

Tummala, H; Collopy, LC; Walne, AJ; Ellison, A; Cardoso, S; Aksu, T; Yarali, N; ... Dokal, I; + view all (2018) Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita like phenotypes. Blood , 132 (12) pp. 1349-1353. 10.1182/blood-2018-03-837799. Green open access

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Type:	Article
Title:	Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita like phenotypes
Location:	United States
Open access status:	An open access version is available from UCL Discovery
DOI:	10.1182/blood-2018-03-837799
Publisher version:	https://doi.org/10.1182/blood-2018-03-837799
Language:	English
Additional information:	This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
UCL classification:	UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > Institute of Ophthalmology UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Cancer Institute UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Cancer Institute > Research Department of Cancer Bio
URI:	https://discovery.ucl.ac.uk/id/eprint/10053887

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