APA (7th ed.) Citation

CL, B., S, D., FJ, A., SU, M., C, S., BD, F., . . . AR, L. S. (2023). Senataxin helicase, the causal gene defect in ALS4, is a significant modifier of C9orf72 ALS G4C2 and arginine-containing dipeptide repeat toxicity. Acta neuropathologica communications, 11(1), 164. https://doi.org/10.1186/s40478-023-01665-z

Chicago Style (17th ed.) Citation

CL, Bennett, et al. "Senataxin Helicase, the Causal Gene Defect in ALS4, Is a Significant Modifier of C9orf72 ALS G4C2 and Arginine-containing Dipeptide Repeat Toxicity." Acta Neuropathologica Communications 11, no. 1 (2023): 164. https://doi.org/10.1186/s40478-023-01665-z.

MLA (9th ed.) Citation

CL, Bennett, et al. "Senataxin Helicase, the Causal Gene Defect in ALS4, Is a Significant Modifier of C9orf72 ALS G4C2 and Arginine-containing Dipeptide Repeat Toxicity." Acta Neuropathologica Communications, vol. 11, no. 1, 2023, p. 164, https://doi.org/10.1186/s40478-023-01665-z.