Cite
Neuropathy due to bi-allelic SH3TC2 variants: genotype-phenotype correlation and natural history.
MLA
Rehbein, Tyler, et al. “Neuropathy Due to Bi-Allelic SH3TC2 Variants: Genotype-Phenotype Correlation and Natural History.” Brain: A Journal of Neurology, vol. 146, no. 9, Sept. 2023, pp. 3826–35. EBSCOhost, https://doi.org/10.1093/brain/awad095.
APA
Rehbein, T., Wu, T. T., Treidler, S., Pareyson, D., Lewis, R., Yum, S. W., McCray, B. A., Ramchandren, S., Burns, J., Li, J., Finkel, R. S., Scherer, S. S., Zuchner, S., Shy, M. E., Reilly, M. M., & Herrmann, D. N. (2023). Neuropathy due to bi-allelic SH3TC2 variants: genotype-phenotype correlation and natural history. Brain: A Journal of Neurology, 146(9), 3826–3835. https://doi.org/10.1093/brain/awad095
Chicago
Rehbein, Tyler, Tong Tong Wu, Simona Treidler, Davide Pareyson, Richard Lewis, Sabrina W Yum, Brett A McCray, et al. 2023. “Neuropathy Due to Bi-Allelic SH3TC2 Variants: Genotype-Phenotype Correlation and Natural History.” Brain: A Journal of Neurology 146 (9): 3826–35. doi:10.1093/brain/awad095.