Cita APA (7a ed.)

Ohmori, T., Nagao, Y., Mizukami, H., Sakata, A., Muramatsu, S., Ozawa, K., . . . Sakata, Y. (2017). CRISPR/Cas9-mediated genome editing via postnatal administration of AAV vector cures haemophilia B mice. Nature Portfolio.

Cita Chicago Style (17a ed.)

Ohmori, Tsukasa, et al. CRISPR/Cas9-mediated Genome Editing via Postnatal Administration of AAV Vector Cures Haemophilia B Mice. Nature Portfolio, 2017.

Cita MLA (8a ed.)

Ohmori, Tsukasa, et al. CRISPR/Cas9-mediated Genome Editing via Postnatal Administration of AAV Vector Cures Haemophilia B Mice. Nature Portfolio, 2017.