Biallelic expansion of an intronic repeat in RFC1is a common cause of late-onset ataxia

MLA

Cortese, Andrea, et al. “Biallelic Expansion of an Intronic Repeat in RFC1is a Common Cause of Late-Onset Ataxia.” Nature Genetics, vol. 51, no. 4, Apr. 2019, pp. 649–58. EBSCOhost, https://doi.org/10.1038/s41588-019-0372-4.

APA

Cortese, A., Simone, R., Sullivan, R., Vandrovcova, J., Tariq, H., Yau, W. Y., Humphrey, J., Jaunmuktane, Z., Sivakumar, P., Polke, J., Ilyas, M., Tribollet, E., Tomaselli, P. J., Devigili, G., Callegari, I., Versino, M., Salpietro, V., Efthymiou, S., Kaski, D., … Houlden, H. (2019). Biallelic expansion of an intronic repeat in RFC1is a common cause of late-onset ataxia. Nature Genetics, 51(4), 649–658. https://doi.org/10.1038/s41588-019-0372-4

Chicago

Cortese, Andrea, Roberto Simone, Roisin Sullivan, Jana Vandrovcova, Huma Tariq, Wai Yan Yau, Jack Humphrey, et al. 2019. “Biallelic Expansion of an Intronic Repeat in RFC1is a Common Cause of Late-Onset Ataxia.” Nature Genetics 51 (4): 649–58. doi:10.1038/s41588-019-0372-4.