TINF2 mutations in children with severe aplastic anemia
Author:
Funder
NIH
Publisher
Wiley
Subject
Oncology,Hematology,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.21903/fullpdf
Reference4 articles.
1. TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita;Savage;Am J Hum Genet,2008
2. TINF2 mutations result in very short telomeres: Analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes;Walne;Blood,2008
3. NOLA1 gene mutations in acquired aplastic anemia;Pigullo;Pediatr Blood Cancer,2008
4. Low frequency of telomerase RNA mutations among children with aplastic anemia or myelodysplastic syndrome;Field;J Pediatr Hematol Oncol,2006
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