APA (7th ed.) Citation

TH, v. P., M, P., L, D., T, G., VJJ, O., M, O., . . . BPC, v. d. W. (2024). A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic Disorder. Movement disorders : official journal of the Movement Disorder Society, 39(9), 1636. https://doi.org/10.1002/mds.29912

Chicago Style (17th ed.) Citation

TH, van Prooije, et al. "A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic Disorder." Movement Disorders : Official Journal of the Movement Disorder Society 39, no. 9 (2024): 1636. https://doi.org/10.1002/mds.29912.

MLA (9th ed.) Citation

TH, van Prooije, et al. "A New Case Series Suggests That SCA48 (ATX/STUB1) Is Primarily a Monogenic Disorder." Movement Disorders : Official Journal of the Movement Disorder Society, vol. 39, no. 9, 2024, p. 1636, https://doi.org/10.1002/mds.29912.