APA (7th ed.) Citation

FA, I., AF, M., A, S., & DM, P. (2012). Spinocerebellar ataxia type 13 mutation that is associated with disease onset in infancy disrupts axonal pathfinding during neuronal development. Disease models & mechanisms, 5(6), 921. https://doi.org/10.1242/dmm.010157

Chicago Style (17th ed.) Citation

FA, Issa, Mock AF, Sagasti A, and Papazian DM. "Spinocerebellar Ataxia Type 13 Mutation That Is Associated with Disease Onset in Infancy Disrupts Axonal Pathfinding During Neuronal Development." Disease Models & Mechanisms 5, no. 6 (2012): 921. https://doi.org/10.1242/dmm.010157.

MLA (9th ed.) Citation

FA, Issa, et al. "Spinocerebellar Ataxia Type 13 Mutation That Is Associated with Disease Onset in Infancy Disrupts Axonal Pathfinding During Neuronal Development." Disease Models & Mechanisms, vol. 5, no. 6, 2012, p. 921, https://doi.org/10.1242/dmm.010157.