APA (7th ed.) Citation

C, S., J, B., J, P., M, G., A, S., JM, D., . . . NJ, A. (2023). CLN2 disease resulting from a novel homozygous deep intronic splice variant in TPP1 discovered using long-read sequencing. Molecular genetics and metabolism, 140(4), 107713. https://doi.org/10.1016/j.ymgme.2023.107713

Chicago Style (17th ed.) Citation

C, Steigerwald, Borsuk J, Pappas J, Galey M, Scott A, Devaney JM, Miller DE, and Abreu NJ. "CLN2 Disease Resulting from a Novel Homozygous Deep Intronic Splice Variant in TPP1 Discovered Using Long-read Sequencing." Molecular Genetics and Metabolism 140, no. 4 (2023): 107713. https://doi.org/10.1016/j.ymgme.2023.107713.

MLA (9th ed.) Citation

C, Steigerwald, et al. "CLN2 Disease Resulting from a Novel Homozygous Deep Intronic Splice Variant in TPP1 Discovered Using Long-read Sequencing." Molecular Genetics and Metabolism, vol. 140, no. 4, 2023, p. 107713, https://doi.org/10.1016/j.ymgme.2023.107713.