Özkılınç Önen, M. Et Al. 2023. Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype. RHEUMATOLOGY , no.9 , 3188-3196.

Özkılınç Önen, M., Onat, U. İ., Uğurlu, S., Timuçin, A. C., Öz Arslan, D., Everest, E., ... Özdoğan, H.(2023). Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype. RHEUMATOLOGY , no.9, 3188-3196.

Özkılınç Önen, Merve Et Al. "Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype," RHEUMATOLOGY , no.9, 3188-3196, 2023

Özkılınç Önen, Merve Ö. Et Al. "Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype." RHEUMATOLOGY , no.9, pp.3188-3196, 2023

Özkılınç Önen, M. Et Al. (2023) . "Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype." RHEUMATOLOGY , no.9, pp.3188-3196.

@article{article, author={Merve Özkılınç Önen Et Al. }, title={Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype}, journal={RHEUMATOLOGY}, year=2023, pages={3188-3196} }