APA (7th ed.) Citation

CK, C., JS, L., KS, L., SK, L., CT, T., & CC, N. (2020). Whole exome sequencing identifies a novel SCN1A mutation in genetic (idiopathic) generalized epilepsy and juvenile myoclonic epilepsy subtypes. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 41(3), 591. https://doi.org/10.1007/s10072-019-04122-9

Chicago Style (17th ed.) Citation

CK, Chan, Low JS, Lim KS, Low SK, Tan CT, and Ng CC. "Whole Exome Sequencing Identifies a Novel SCN1A Mutation in Genetic (idiopathic) Generalized Epilepsy and Juvenile Myoclonic Epilepsy Subtypes." Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 41, no. 3 (2020): 591. https://doi.org/10.1007/s10072-019-04122-9.

MLA (9th ed.) Citation

CK, Chan, et al. "Whole Exome Sequencing Identifies a Novel SCN1A Mutation in Genetic (idiopathic) Generalized Epilepsy and Juvenile Myoclonic Epilepsy Subtypes." Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, vol. 41, no. 3, 2020, p. 591, https://doi.org/10.1007/s10072-019-04122-9.