APA (7th ed.) Citation

Hartmann, J., & Monyer, H. (2019). GluA4-targeted AAV vectors deliver genes selectively to interneurons while relying on the AAV receptor for entry. Molecular therapy. Methods & clinical development, 14, . https://doi.org/10.1016/j.omtm.2019.07.004

Chicago Style (17th ed.) Citation

Hartmann, Jessica, and Hannah Monyer. "GluA4-targeted AAV Vectors Deliver Genes Selectively to Interneurons While Relying on the AAV Receptor for Entry." Molecular Therapy. Methods & Clinical Development 14 (2019). https://doi.org/10.1016/j.omtm.2019.07.004.

MLA (9th ed.) Citation

Hartmann, Jessica, and Hannah Monyer. "GluA4-targeted AAV Vectors Deliver Genes Selectively to Interneurons While Relying on the AAV Receptor for Entry." Molecular Therapy. Methods & Clinical Development, vol. 14, 2019, https://doi.org/10.1016/j.omtm.2019.07.004.