Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48).

MLA

Hirst, Jennifer, et al. “Complicated Spastic Paraplegia in Patients with AP5Z1 Mutations (SPG48).” Neurology. Genetics, vol. 2, no. 5, Aug. 2016, p. e98. EBSCOhost, https://doi.org/10.1212/NXG.0000000000000098.

APA

Hirst, J., Madeo, M., Smets, K., Edgar, J. R., Schols, L., Li, J., Yarrow, A., Deconinck, T., Baets, J., Van Aken, E., De Bleecker, J., Datiles, M. B., 3rd, Roda, R. H., Liepert, J., Züchner, S., Mariotti, C., De Jonghe, P., Blackstone, C., & Kruer, M. C. (2016). Complicated spastic paraplegia in patients with AP5Z1 mutations (SPG48). Neurology. Genetics, 2(5), e98. https://doi.org/10.1212/NXG.0000000000000098

Chicago

Hirst, Jennifer, Marianna Madeo, Katrien Smets, James R Edgar, Ludger Schols, Jun Li, Anna Yarrow, et al. 2016. “Complicated Spastic Paraplegia in Patients with AP5Z1 Mutations (SPG48).” Neurology. Genetics 2 (5): e98. doi:10.1212/NXG.0000000000000098.