Cite
Novel De Novo Mutations in KIF1A as a Cause of Hereditary Spastic Paraplegia With Progressive Central Nervous System Involvement.
MLA
Hotchkiss, Leslie, et al. “Novel De Novo Mutations in KIF1A as a Cause of Hereditary Spastic Paraplegia With Progressive Central Nervous System Involvement.” Journal of Child Neurology, vol. 31, no. 9, Aug. 2016, pp. 1114–19. EBSCOhost, https://doi.org/10.1177/0883073816639718.
APA
Hotchkiss, L., Donkervoort, S., Leach, M. E., Mohassel, P., Bharucha-Goebel, D. X., Bradley, N., Nguyen, D., Hu, Y., Gurgel-Giannetti, J., & Bönnemann, C. G. (2016). Novel De Novo Mutations in KIF1A as a Cause of Hereditary Spastic Paraplegia With Progressive Central Nervous System Involvement. Journal of Child Neurology, 31(9), 1114–1119. https://doi.org/10.1177/0883073816639718
Chicago
Hotchkiss, Leslie, Sandra Donkervoort, Meganne E. Leach, Payam Mohassel, Diana X. Bharucha-Goebel, Nathaniel Bradley, David Nguyen, Ying Hu, Juliana Gurgel-Giannetti, and Carsten G. Bönnemann. 2016. “Novel De Novo Mutations in KIF1A as a Cause of Hereditary Spastic Paraplegia With Progressive Central Nervous System Involvement.” Journal of Child Neurology 31 (9): 1114–19. doi:10.1177/0883073816639718.