Cita APA (7a ed.)
Önen, M. Ö., Onat, U. İ., Uğurlu, S., Timuçin, A. C., Arslan, D. Ö., Everest, E., . . . Turanlı, E. T. (2023). Detection of a rare variant in PSTPIP1 through three generations in a family with an initial diagnosis of FMF/MKD-overlapping phenotype. Rheumatology, 62(9), 3188-3197.
Cita Chicago Style (17a ed.)
Önen, Merve Özkılınç, Umut İ Onat, Serdal Uğurlu, Ahmet C. Timuçin, Devrim Öz Arslan, Elif Everest, Huri Özdoğan, y Eda Tahir Turanlı. "Detection of a Rare Variant in PSTPIP1 Through Three Generations in a Family with an Initial Diagnosis of FMF/MKD-overlapping Phenotype." Rheumatology 62, no. 9 (2023): 3188-3197.
Cita MLA (9a ed.)
Önen, Merve Özkılınç, 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, vol. 62, no. 9, 2023, pp. 3188-3197.
Precaución: Estas citas no son 100% exactas.