TINF2 Mutations in Children With Severe Aplastic Anemia

被引:28
作者
Du, Hong-Yan [2 ]
Mason, Philip J. [2 ,3 ]
Bessler, Monica [2 ,4 ]
Wilson, David B. [1 ,4 ]
机构
[1] Washington Univ, Sch Med, Dept Pediat, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Internal Med, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Dev Biol, St Louis, MO 63110 USA
关键词
DYSKERATOSIS-CONGENITA;
D O I
10.1002/pbc.21903
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
引用
收藏
页码:687 / 687
页数:1
相关论文
共 4 条
  • [1] Low frequency of telomerase RNA mutations among children with aplastic anemia or myelodysplastic syndrome
    Field, Joshua J.
    Mason, Philip J.
    An, Ping
    Kasai, Yumi
    McLellan, Michael
    Jaeger, Sara
    Barnes, Yvonne J.
    King, Allison A.
    Bessler, Monica
    Wilson, David B.
    [J]. JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY, 2006, 28 (07) : 450 - 453
  • [2] PIGULLO S, 2008, PEDIAT BLOO IN PRESS
  • [3] TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenita
    Savage, Sharon A.
    Giri, Neelarn
    Baerlocher, Gabriela M.
    Orr, Nick
    Lansdorp, Peter M.
    Alter, Blanche P.
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2008, 82 (02) : 501 - 509
  • [4] TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes
    Walne, Amanda J.
    Vulliamy, Tom
    Beswick, Richard
    Kirwan, Michael
    Dokal, Inderjeet
    [J]. BLOOD, 2008, 112 (09) : 3594 - 3600