ÖZEN, S. Et Al. 2020. A monogenic disease with a variety of phenotypes: Deficiency of adenosine deaminase 2. Journal of Rheumatology , vol.47, no.1 , 117-125.

ÖZEN, S., BATU AKAL, E. D., Taşkiran, E. Z., ÖZKARA, H. A., Ünal, Ş., Güleray, N., ... Erden, A.(2020). A monogenic disease with a variety of phenotypes: Deficiency of adenosine deaminase 2. Journal of Rheumatology , vol.47, no.1, 117-125.

ÖZEN, SEZA Et Al. "A monogenic disease with a variety of phenotypes: Deficiency of adenosine deaminase 2," Journal of Rheumatology , vol.47, no.1, 117-125, 2020

ÖZEN, SEZA Et Al. "A monogenic disease with a variety of phenotypes: Deficiency of adenosine deaminase 2." Journal of Rheumatology , vol.47, no.1, pp.117-125, 2020

ÖZEN, S. Et Al. (2020) . "A monogenic disease with a variety of phenotypes: Deficiency of adenosine deaminase 2." Journal of Rheumatology , vol.47, no.1, pp.117-125.

@article{article, author={SEZA ÖZEN Et Al. }, title={A monogenic disease with a variety of phenotypes: Deficiency of adenosine deaminase 2}, journal={Journal of Rheumatology}, year=2020, pages={117-125} }