APA (7th ed.) Citation

AM, R., GL, D., J, B., JM, P., SM, M., H, H., . . . MM, R. (2012). A novel p.Gln175X [corrected] premature stop mutation in the C-terminal end of HSP27 is a cause of CMT2. Journal of the peripheral nervous system : JPNS, 17(2), 201. https://doi.org/10.1111/j.1529-8027.2012.00400.x

Chicago Style (17th ed.) Citation

AM, Rossor, et al. "A Novel P.Gln175X [corrected] Premature Stop Mutation in the C-terminal End of HSP27 Is a Cause of CMT2." Journal of the Peripheral Nervous System : JPNS 17, no. 2 (2012): 201. https://doi.org/10.1111/j.1529-8027.2012.00400.x.

MLA (9th ed.) Citation

AM, Rossor, et al. "A Novel P.Gln175X [corrected] Premature Stop Mutation in the C-terminal End of HSP27 Is a Cause of CMT2." Journal of the Peripheral Nervous System : JPNS, vol. 17, no. 2, 2012, p. 201, https://doi.org/10.1111/j.1529-8027.2012.00400.x.