Mutations in telomerase catalytic protein in Japanese children with aplastic anemia

Juan Liang, Hiroshi Yagasaki, Yoshiro Kamachi, Asahito Hama, Kimikazu Matsumoto, Kouji Kato, Kazuko Kudo, Seiji Kojima

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38 Citations (Scopus)

Abstract

Recent studies indicate that a subset of patients with apparently acquired aplastic anemia (AA) have mutations in genes for telomerase ribonucleoprotein complex components. We looked for mutations in telomerase RNA (TERC) and telomerase reverse transcriptase (TERT) in 96 Japanese children with acquired AA and in 76 healthy controls. No mutations in TERC were found in any subjects. Novel heterozygous, non-synonymous mutations in TERT (T726M and G682D) were found in two patients with AA, neither of whom had clinical characteristics suggesting constitutional AA. This genetic difference does not explain the higher incidence of AA in Asian populations.

Original languageEnglish
Pages (from-to)656-658
Number of pages3
JournalHaematologica
Volume91
Issue number5
Publication statusPublished - May 1 2006
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Hematology

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  • Cite this

    Liang, J., Yagasaki, H., Kamachi, Y., Hama, A., Matsumoto, K., Kato, K., Kudo, K., & Kojima, S. (2006). Mutations in telomerase catalytic protein in Japanese children with aplastic anemia. Haematologica, 91(5), 656-658.