A multi-exon RFC1 deletion in a case of CANVAS: expanding the genetic mechanism of disease.

MLA

Davies, Kayli C., et al. “A Multi-Exon RFC1 Deletion in a Case of CANVAS: Expanding the Genetic Mechanism of Disease.” Journal of Neurology, vol. 271, no. 12, Dec. 2024, pp. 7622–27. EBSCOhost, https://doi.org/10.1007/s00415-024-12675-9.

APA

Davies, K. C., Fearnley, L. G., Snell, P., Bourke, D., Mossman, S., Kyne, K., McKeown, C., Delatycki, M. B., Bahlo, M., & Lockhart, P. J. (2024). A multi-exon RFC1 deletion in a case of CANVAS: expanding the genetic mechanism of disease. Journal of Neurology, 271(12), 7622–7627. https://doi.org/10.1007/s00415-024-12675-9

Chicago

Davies, Kayli C., Liam G. Fearnley, Penny Snell, David Bourke, Stuart Mossman, Karen Kyne, Colina McKeown, Martin B. Delatycki, Melanie Bahlo, and Paul J. Lockhart. 2024. “A Multi-Exon RFC1 Deletion in a Case of CANVAS: Expanding the Genetic Mechanism of Disease.” Journal of Neurology 271 (12): 7622–27. doi:10.1007/s00415-024-12675-9.