Cite
TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila.
MLA
Goodman, Lindsey D., et al. “TNPO2 Variants Associate with Human Developmental Delays, Neurologic Deficits, and Dysmorphic Features and Alter TNPO2 Activity in Drosophila.” American Journal of Human Genetics, vol. 108, no. 9, Sept. 2021, pp. 1669–91. EBSCOhost, https://doi.org/10.1016/j.ajhg.2021.06.019.
APA
Goodman, L. D., Cope, H., Nil, Z., Ravenscroft, T. A., Charng, W.-L., Lu, S., Tien, A.-C., Pfundt, R., Koolen, D. A., Haaxma, C. A., Veenstra-Knol, H. E., Wassink-Ruiter, J. S. K., Wevers, M. R., Jones, M., Walsh, L. E., Klee, V. H., Theunis, M., Legius, E., Steel, D., … Tan, Q. K.-G. (2021). TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila. American Journal of Human Genetics, 108(9), 1669–1691. https://doi.org/10.1016/j.ajhg.2021.06.019
Chicago
Goodman, Lindsey D, Heidi Cope, Zelha Nil, Thomas A Ravenscroft, Wu-Lin Charng, Shenzhao Lu, An-Chi Tien, et al. 2021. “TNPO2 Variants Associate with Human Developmental Delays, Neurologic Deficits, and Dysmorphic Features and Alter TNPO2 Activity in Drosophila.” American Journal of Human Genetics 108 (9): 1669–91. doi:10.1016/j.ajhg.2021.06.019.