APA (7th ed.) Citation

Barbier, M., Bahlo, M., Pennisi, A., Jacoupy, M., Tankard, R. M., Ewenczyk, C., . . . Gardner, R. J. M. (2022). Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25. Annals of Neurology, 92(1), 122. https://doi.org/10.1002/ana.26366

Chicago Style (17th ed.) Citation

Barbier, Mathieu, et al. "Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25." Annals of Neurology 92, no. 1 (2022): 122. https://doi.org/10.1002/ana.26366.

MLA (9th ed.) Citation

Barbier, Mathieu, et al. "Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25." Annals of Neurology, vol. 92, no. 1, 2022, p. 122, https://doi.org/10.1002/ana.26366.