Cite
Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer's disease: a case series.
MLA
Ryan, Natalie S., et al. “Clinical Phenotype and Genetic Associations in Autosomal Dominant Familial Alzheimer’s Disease: A Case Series.” Lancet Neurology, vol. 15, no. 13, Dec. 2016, pp. 1326–35. EBSCOhost, https://doi.org/10.1016/S1474-4422(16)30193-4.
APA
Ryan, N. S., Nicholas, J. M., Weston, P. S. J., Liang, Y., Lashley, T., Guerreiro, R., Adamson, G., Kenny, J., Beck, J., Chavez-Gutierrez, L., de Strooper, B., Revesz, T., Holton, J., Mead, S., Rossor, M. N., & Fox, N. C. (2016). Clinical phenotype and genetic associations in autosomal dominant familial Alzheimer’s disease: a case series. Lancet Neurology, 15(13), 1326–1335. https://doi.org/10.1016/S1474-4422(16)30193-4
Chicago
Ryan, Natalie S, Jennifer M Nicholas, Philip S J Weston, Yuying Liang, Tammaryn Lashley, Rita Guerreiro, Gary Adamson, et al. 2016. “Clinical Phenotype and Genetic Associations in Autosomal Dominant Familial Alzheimer’s Disease: A Case Series.” Lancet Neurology 15 (13): 1326–35. doi:10.1016/S1474-4422(16)30193-4.