APA (7th ed.) Citation

Cousin, M. A., Veale, E. L., Dsouza, N. R., Tripathi, S., Holden, R. G., Arelin, M., . . . Ferlini, A. (2022). Gain and loss of TASK3 channel function and its regulation by novel variation cause KCNK9 imprinting syndrome. Genome Medicine, 14(1), 1. https://doi.org/10.1186/s13073-022-01064-4

Chicago Style (17th ed.) Citation

Cousin, Margot A., et al. "Gain and Loss of TASK3 Channel Function and Its Regulation by Novel Variation Cause KCNK9 Imprinting Syndrome." Genome Medicine 14, no. 1 (2022): 1. https://doi.org/10.1186/s13073-022-01064-4.

MLA (9th ed.) Citation

Cousin, Margot A., et al. "Gain and Loss of TASK3 Channel Function and Its Regulation by Novel Variation Cause KCNK9 Imprinting Syndrome." Genome Medicine, vol. 14, no. 1, 2022, p. 1, https://doi.org/10.1186/s13073-022-01064-4.