APA (7th ed.) Citation

Donkervoort, S., Mohassel, P., O'Leary, M., Bonner, D. E., Hartley, T., Acquaye, N., . . . Acosta, M. T. (2024). Recurring homozygous ACTN2 variant (p.Arg506Gly) causes a recessive myopathy. Annals of Clinical & Translational Neurology, 11(3), 629. https://doi.org/10.1002/acn3.51983

Chicago Style (17th ed.) Citation

Donkervoort, Sandra, et al. "Recurring Homozygous ACTN2 Variant (p.Arg506Gly) Causes a Recessive Myopathy." Annals of Clinical & Translational Neurology 11, no. 3 (2024): 629. https://doi.org/10.1002/acn3.51983.

MLA (9th ed.) Citation

Donkervoort, Sandra, et al. "Recurring Homozygous ACTN2 Variant (p.Arg506Gly) Causes a Recessive Myopathy." Annals of Clinical & Translational Neurology, vol. 11, no. 3, 2024, p. 629, https://doi.org/10.1002/acn3.51983.