APA (7th ed.) Citation

S, S., Y, L., G, Y., J, A., I, B., A, B., . . . K, B. (2021). Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia. Genetics in medicine : official journal of the American College of Medical Genetics, 23(2), 341. https://doi.org/10.1038/s41436-020-00979-w

Chicago Style (17th ed.) Citation

S, Schröder, et al. "Heterozygous Truncating Variants in SUFU Cause Congenital Ocular Motor Apraxia." Genetics in Medicine : Official Journal of the American College of Medical Genetics 23, no. 2 (2021): 341. https://doi.org/10.1038/s41436-020-00979-w.

MLA (9th ed.) Citation

S, Schröder, et al. "Heterozygous Truncating Variants in SUFU Cause Congenital Ocular Motor Apraxia." Genetics in Medicine : Official Journal of the American College of Medical Genetics, vol. 23, no. 2, 2021, p. 341, https://doi.org/10.1038/s41436-020-00979-w.