APA (7th ed.) Citation

Spaull, R., Steel, D., Barwick, K., Prabhakar, P., Wakeling, E., & Kurian, M. A. (2022). STXBP1 Stop‐Loss Mutation Associated with Complex Early Onset Movement Disorder without Epilepsy. Movement disorders clinical practice (Hoboken, N.J.), 9(6), 837-840. https://doi.org/10.1002/mdc3.13509

Chicago Style (17th ed.) Citation

Spaull, Robert, Dora Steel, Katy Barwick, Prab Prabhakar, Emma Wakeling, and Manju A. Kurian. "STXBP1 Stop‐Loss Mutation Associated with Complex Early Onset Movement Disorder Without Epilepsy." Movement Disorders Clinical Practice (Hoboken, N.J.) 9, no. 6 (2022): 837-840. https://doi.org/10.1002/mdc3.13509.

MLA (9th ed.) Citation

Spaull, Robert, et al. "STXBP1 Stop‐Loss Mutation Associated with Complex Early Onset Movement Disorder Without Epilepsy." Movement Disorders Clinical Practice (Hoboken, N.J.), vol. 9, no. 6, 2022, pp. 837-840, https://doi.org/10.1002/mdc3.13509.