Cite
A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts
MLA
Ingre, Caroline, et al. “A Novel Phosphorylation Site Mutation in Profilin 1 Revealed in a Large Screen of US, Nordic, and German Amyotrophic Lateral Sclerosis/Frontotemporal Dementia Cohorts.” Neurobiology of Aging, vol. 34, no. 6, June 2013, p. 1708.e1-1708.e6. EBSCOhost, https://doi.org/10.1016/j.neurobiolaging.2012.10.009.
APA
Ingre, C., Landers, J. E., Rizik, N., Volk, A. E., Akimoto, C., Birve, A., Hübers, A., Keagle, P. J., Piotrowska, K., Press, R., Andersen, P. M., Ludolph, A. C., & Weishaupt, J. H. (2013). A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts. Neurobiology of Aging, 34(6), 1708.e1-1708.e6. https://doi.org/10.1016/j.neurobiolaging.2012.10.009
Chicago
Ingre, Caroline, John E. Landers, Naji Rizik, Alexander E. Volk, Chizuru Akimoto, Anna Birve, Annemarie Hübers, et al. 2013. “A Novel Phosphorylation Site Mutation in Profilin 1 Revealed in a Large Screen of US, Nordic, and German Amyotrophic Lateral Sclerosis/Frontotemporal Dementia Cohorts.” Neurobiology of Aging 34 (6): 1708.e1-1708.e6. doi:10.1016/j.neurobiolaging.2012.10.009.