Expansion of the phenotypic spectrum of de novo missense variants in kinesin family member 1A (KIF1A).

MLA

Kaur, Simranpreet, et al. “Expansion of the Phenotypic Spectrum of de Novo Missense Variants in Kinesin Family Member 1A (KIF1A).” Human Mutation, vol. 41, no. 10, Oct. 2020, pp. 1761–74. EBSCOhost, https://doi.org/10.1002/humu.24079.

APA

Kaur, S., Van Bergen, N. J., Verhey, K. J., Nowell, C. J., Budaitis, B., Yue, Y., Ellaway, C., Brunetti-Pierri, N., Cappuccio, G., Bruno, I., Boyle, L., Nigro, V., Torella, A., Roscioli, T., Cowley, M. J., Massey, S., Sonawane, R., Burton, M. D., Schonewolf-Greulich, B., … Christodoulou, J. (2020). Expansion of the phenotypic spectrum of de novo missense variants in kinesin family member 1A (KIF1A). Human Mutation, 41(10), 1761–1774. https://doi.org/10.1002/humu.24079

Chicago

Kaur, Simranpreet, Nicole J Van Bergen, Kristen J Verhey, Cameron J Nowell, Breane Budaitis, Yang Yue, Carolyn Ellaway, et al. 2020. “Expansion of the Phenotypic Spectrum of de Novo Missense Variants in Kinesin Family Member 1A (KIF1A).” Human Mutation 41 (10): 1761–74. doi:10.1002/humu.24079.