APA način citiranja (7. izdanje)

Dias, C., Punetha, J., Zheng, C., Mazaheri, N., Rad, A., Efthymiou, S., . . . Maroofian, R. (2019). Homozygous missense variants in NTNG2, encoding a presynaptic netrin-G2 adhesion protein, lead to a distinct neurodevelopmental disorder. Elsevier.

Čikaški stil citiranja (17. izdanje)

Dias, CM, et al. Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. Elsevier, 2019.

MLA način citiranja (9. izdanje)

Dias, CM, et al. Homozygous Missense Variants in NTNG2, Encoding a Presynaptic Netrin-G2 Adhesion Protein, Lead to a Distinct Neurodevelopmental Disorder. Elsevier, 2019.