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Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypes
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Blizard Institute
Centre for Genomics and Child Health
Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypes
QMRO Home
Blizard Institute
Centre for Genomics and Child Health
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
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Accepted version (74.20Kb)
Volume
132
Pagination
1349 - 1353
DOI
10.1182/blood-2018-03-837799
Journal
BLOOD
Issue
12
ISSN
0006-4971
Metadata
Show full item record
Authors
Tummala, H; Collopy, LC; Walne, AJ; Ellison, A; Cardoso, S; Aksu, T; Yarali, N; Aslan, D; Akata, RF; Teo, J
URI
http://qmro.qmul.ac.uk/xmlui/handle/123456789/42823
Collections
Centre for Genomics and Child Health
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© 2018 American Society of Hematology