Kisla, E. Et Al. 2017. A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis.. European journal of medical genetics , vol.60 , 690-694.

Kisla, E., Balci, S., Bisgin, A., Altintas, D. U., & Yilmaz, M., (2017). A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis.. European journal of medical genetics , vol.60, 690-694.

Kisla, RABİA Et Al. "A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis.," European journal of medical genetics , vol.60, 690-694, 2017

Kisla, RABİA M. Et Al. "A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis.." European journal of medical genetics , vol.60, pp.690-694, 2017

Kisla, E. Et Al. (2017) . "A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis.." European journal of medical genetics , vol.60, pp.690-694.

@article{article, author={RABİA MİRAY KIŞLA EKİNCİ Et Al. }, title={A homozygote TREX1 mutation in two siblings with different phenotypes: Chilblains and cerebral vasculitis.}, journal={European journal of medical genetics}, year=2017, pages={690-694} }