Shin, J. W., Hong, E. P., Park, S. S., Choi, D. E., Zeng, S., Chen, R. Z., & Lee, J. (2022). PAM-altering SNP-based allele-specific CRISPR-Cas9 therapeutic strategies for Huntington’s disease. Molecular therapy. Methods & clinical development, 26, 547-561. https://doi.org/10.1016/j.omtm.2022.08.005
Chicago Style (17th ed.) CitationShin, Jun Wan, Eun Pyo Hong, Seri S. Park, Doo Eun Choi, Sophia Zeng, Richard Z. Chen, and Jong-Min Lee. "PAM-altering SNP-based Allele-specific CRISPR-Cas9 Therapeutic Strategies for Huntington’s Disease." Molecular Therapy. Methods & Clinical Development 26 (2022): 547-561. https://doi.org/10.1016/j.omtm.2022.08.005.
MLA (9th ed.) CitationShin, Jun Wan, et al. "PAM-altering SNP-based Allele-specific CRISPR-Cas9 Therapeutic Strategies for Huntington’s Disease." Molecular Therapy. Methods & Clinical Development, vol. 26, 2022, pp. 547-561, https://doi.org/10.1016/j.omtm.2022.08.005.