Cite
Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions.
MLA
Lattante, Serena, et al. “Defining the Association of TMEM106B Variants among Frontotemporal Lobar Degeneration Patients with GRN Mutations and C9orf72 Repeat Expansions.” Neurobiology of Aging, vol. 35, no. 11, Nov. 2014, p. 2658.e1-2658.e5. EBSCOhost, https://doi.org/10.1016/j.neurobiolaging.2014.06.023.
APA
Lattante, S., Le Ber, I., Galimberti, D., Serpente, M., Rivaud-Péchoux, S., Camuzat, A., Clot, F., Fenoglio, C., Scarpini, E., Brice, A., & Kabashi, E. (2014). Defining the association of TMEM106B variants among frontotemporal lobar degeneration patients with GRN mutations and C9orf72 repeat expansions. Neurobiology of Aging, 35(11), 2658.e1-2658.e5. https://doi.org/10.1016/j.neurobiolaging.2014.06.023
Chicago
Lattante, Serena, Isabelle Le Ber, Daniela Galimberti, Maria Serpente, Sophie Rivaud-Péchoux, Agnès Camuzat, Fabienne Clot, et al. 2014. “Defining the Association of TMEM106B Variants among Frontotemporal Lobar Degeneration Patients with GRN Mutations and C9orf72 Repeat Expansions.” Neurobiology of Aging 35 (11): 2658.e1-2658.e5. doi:10.1016/j.neurobiolaging.2014.06.023.