Archives of Dermatological Research

, Volume 302, Issue 3, pp 235–236 | Cite as

Identification of two novel DSRAD mutations in two Chinese families with dyschromatosis symmetrica hereditaria

  • Qingqiang Xu
  • Shengxiang Xiao
  • Jia Huo
  • Yingying Dong
  • Jianwen Ren
  • Xiaopeng Wang
  • Junhong Ma
  • Jingang An
  • Yan Liu
Letter to the Editor
First Online:
Received:
Accepted:

Keywords

Intronic Sequence Adenosine Deaminase Chinese Family Dorsal Aspect Common Polymorphism 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
This is a preview of subscription content, log in to check access.

Notes

Acknowledgments

This work was funded by Grants from the National Natural Science Foundation of China (30800991) and the Doctoral Fund of Ministry of Education of China (200806981034). We sincerely thank the member of families for their collaboration.

References

  1. 1.
    Li M, Yang LJ, Shi YX, Huang HY (2007) A novel missense mutation in DSRAD in a family with dyschromatosis symmetrica hereditaria. Arch Dermatol Res 299:273–275CrossRefPubMedGoogle Scholar
  2. 2.
    Liu Q, Liu WL, Jiang L et al (2004) Novel mutations of the RNA-specific adenosine deaminase gene (DSRAD) in Chinese families with dyschromatosis symmetrica hereditaria. J Invest Dermatol 122:896–899CrossRefPubMedGoogle Scholar
  3. 3.
    Liu Y, Xiao SX, Peng ZH et al (2006) A new mutation of the double-stranded RNA-specific adenosine deaminase gene in a family with dyschromatosis symmetrica hereditaria. Dermatology 213:200–203CrossRefPubMedGoogle Scholar
  4. 4.
    Miyamura Y, Suzuki T, Kono M et al (2003) Mutations of RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria. Am J Hum Genet 73:693–699CrossRefPubMedGoogle Scholar
  5. 5.
    Oyama M, Shimizu H, Ohata Y et al (1999) Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases. Br J Dermatol 140:491–496CrossRefPubMedGoogle Scholar
  6. 6.
    Schade M, Turner CJ, Kuhne R et al (1999) The solution structure of the Z-alpha domain of the human RNA editing enzyme ADAR1 reveals a prepositioned binding surface for Z-DNA. Proc Natl Acad Sci USA 96:12465–12470CrossRefPubMedGoogle Scholar
  7. 7.
    Zhang XJ, Gao M, Li M et al (2003) Identification of a locus for dyschromatosis symmetrica hereditaria at chromosome 1q11–1q21. J Invest Dermatol 120:776–780CrossRefPubMedGoogle Scholar

Copyright information

© Springer-Verlag 2010

Authors and Affiliations

  • Qingqiang Xu
    • 1
  • Shengxiang Xiao
    • 1
  • Jia Huo
    • 1
  • Yingying Dong
    • 1
  • Jianwen Ren
    • 1
  • Xiaopeng Wang
    • 1
  • Junhong Ma
    • 1
  • Jingang An
    • 1
  • Yan Liu
    • 1
  1. 1.Department of Dermatology, Second HospitalXi’an Jiaotong UniversityXi’anPeople’s Republic of China

Personalised recommendations