Characterization of spastic paraplegia in a family with a novel PSEN1 mutation.

MLA

Ringman, John M., et al. “Characterization of Spastic Paraplegia in a Family with a Novel PSEN1 Mutation.” Brain Communications, vol. 5, no. 2, Feb. 2023, p. fcad030. EBSCOhost, https://doi.org/10.1093/braincomms/fcad030.

APA

Ringman, J. M., Dorrani, N., Fernández, S. G., Signer, R., Martinez-Agosto, J., Lee, H., Douine, E. D., Qiao, Y., Shi, Y., D’Orazio, L., Pawar, S., Robbie, L., Kashani, A. H., Singer, M., Byers, J. T., Magaki, S., Guzman, S., Sagare, A., Zlokovic, B., … Vinters, H. V. (2023). Characterization of spastic paraplegia in a family with a novel PSEN1 mutation. Brain Communications, 5(2), fcad030. https://doi.org/10.1093/braincomms/fcad030

Chicago

Ringman, John M, Naghmeh Dorrani, Sara Gutiérrez Fernández, Rebecca Signer, Julian Martinez-Agosto, Hane Lee, Emilie D Douine, et al. 2023. “Characterization of Spastic Paraplegia in a Family with a Novel PSEN1 Mutation.” Brain Communications 5 (2): fcad030. doi:10.1093/braincomms/fcad030.