APA (7th ed.) Citation

Lompré, A., Hadri, L., Merlet, E., Keuylian, Z., Mougenot, N., Karakikes, I., . . . Lipskaia, L. (2013). Efficient transduction of vascular smooth muscle cells with a translational AAV2.5 vector: A new perspective for in-stent restenosis gene therapy. Gene Therapy, 20(9), 901. https://doi.org/10.1038/gt.2013.13

Chicago Style (17th ed.) Citation

Lompré, A-M, et al. "Efficient Transduction of Vascular Smooth Muscle Cells with a Translational AAV2.5 Vector: A New Perspective for In-stent Restenosis Gene Therapy." Gene Therapy 20, no. 9 (2013): 901. https://doi.org/10.1038/gt.2013.13.

MLA (9th ed.) Citation

Lompré, A-M, et al. "Efficient Transduction of Vascular Smooth Muscle Cells with a Translational AAV2.5 Vector: A New Perspective for In-stent Restenosis Gene Therapy." Gene Therapy, vol. 20, no. 9, 2013, p. 901, https://doi.org/10.1038/gt.2013.13.