Cite
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations.
MLA
Polke, J. M., et al. “Recessive Axonal Charcot-Marie-Tooth Disease Due to Compound Heterozygous Mitofusin 2 Mutations.” Neurology, vol. 77, no. 2, July 2011, pp. 168–73. EBSCOhost, https://doi.org/10.1212/WNL.0b013e3182242d4d.
APA
Polke, J. M., Laurá, M., Pareyson, D., Taroni, F., Milani, M., Bergamin, G., Gibbons, V. S., Houlden, H., Chamley, S. C., Blake, J., Devile, C., Sandford, R., Sweeney, M. G., Davis, M. B., & Reilly, M. M. (2011). Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations. Neurology, 77(2), 168–173. https://doi.org/10.1212/WNL.0b013e3182242d4d
Chicago
Polke, J M, M Laurá, D Pareyson, F Taroni, M Milani, G Bergamin, V S Gibbons, et al. 2011. “Recessive Axonal Charcot-Marie-Tooth Disease Due to Compound Heterozygous Mitofusin 2 Mutations.” Neurology 77 (2): 168–73. doi:10.1212/WNL.0b013e3182242d4d.