APA (7th ed.) Citation

K, H., L, P., J, N., AHH, N., K, H., AL, N., . . . N, L. (2020). Human Lentiviral Gene Therapy Restores the Cellular Phenotype of Autosomal Recessive Complete IFN-γR1 Deficiency. Molecular therapy. Methods & clinical development, 17, 785. https://doi.org/10.1016/j.omtm.2020.04.002

Chicago Style (17th ed.) Citation

K, Hahn, et al. "Human Lentiviral Gene Therapy Restores the Cellular Phenotype of Autosomal Recessive Complete IFN-γR1 Deficiency." Molecular Therapy. Methods & Clinical Development 17 (2020): 785. https://doi.org/10.1016/j.omtm.2020.04.002.

MLA (9th ed.) Citation

K, Hahn, et al. "Human Lentiviral Gene Therapy Restores the Cellular Phenotype of Autosomal Recessive Complete IFN-γR1 Deficiency." Molecular Therapy. Methods & Clinical Development, vol. 17, 2020, p. 785, https://doi.org/10.1016/j.omtm.2020.04.002.