APA (7th ed.) Citation

JC, M., P, N., S, G., L, D., X, I., JM, M., . . . IE, S. (2006). A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A. Neurology, 67(6), 1094. https://doi.org/10.1212/01.wnl.0000237322.04338.2b

Chicago Style (17th ed.) Citation

JC, Mulley, et al. "A New Molecular Mechanism for Severe Myoclonic Epilepsy of Infancy: Exonic Deletions in SCN1A." Neurology 67, no. 6 (2006): 1094. https://doi.org/10.1212/01.wnl.0000237322.04338.2b.

MLA (9th ed.) Citation

JC, Mulley, et al. "A New Molecular Mechanism for Severe Myoclonic Epilepsy of Infancy: Exonic Deletions in SCN1A." Neurology, vol. 67, no. 6, 2006, p. 1094, https://doi.org/10.1212/01.wnl.0000237322.04338.2b.