A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis.


Kisla E. , Balci S. , Bisgin A. , Altintas D. U. , Yilmaz M.

European journal of medical genetics, vol.60, pp.690-694, 2017 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 60
  • Publication Date: 2017
  • Doi Number: 10.1016/j.ejmg.2017.09.004
  • Title of Journal : European journal of medical genetics
  • Page Numbers: pp.690-694