Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France.

MLA

Lattante, Serena, et al. “Mutations in the PFN1 Gene Are Not a Common Cause in Patients with Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration in France.” Neurobiology of Aging, vol. 34, no. 6, June 2013, p. 1709.e1-2. EBSCOhost, https://doi.org/10.1016/j.neurobiolaging.2012.10.026.

APA

Lattante, S., Le Ber, I., Camuzat, A., Brice, A., & Kabashi, E. (2013). Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France. Neurobiology of Aging, 34(6), 1709.e1-2. https://doi.org/10.1016/j.neurobiolaging.2012.10.026

Chicago

Lattante, Serena, Isabelle Le Ber, Agnès Camuzat, Alexis Brice, and Edor Kabashi. 2013. “Mutations in the PFN1 Gene Are Not a Common Cause in Patients with Amyotrophic Lateral Sclerosis and Frontotemporal Lobar Degeneration in France.” Neurobiology of Aging 34 (6): 1709.e1-2. doi:10.1016/j.neurobiolaging.2012.10.026.