APA (7th ed.) Citation

Brunet, T., Zott, B., Lieftüchter, V., Lenz, D., Schmidt, A., Peters, P., . . . Wagner, M. (2024). De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset stroke. Genetics in medicine, 26(2), . https://doi.org/10.1016/j.gim.2023.101013

Chicago Style (17th ed.) Citation

Brunet, Theresa, et al. "De Novo Variants in RNF213 Are Associated with a Clinical Spectrum Ranging from Leigh Syndrome to Early-onset Stroke." Genetics in Medicine 26, no. 2 (2024). https://doi.org/10.1016/j.gim.2023.101013.

MLA (9th ed.) Citation

Brunet, Theresa, et al. "De Novo Variants in RNF213 Are Associated with a Clinical Spectrum Ranging from Leigh Syndrome to Early-onset Stroke." Genetics in Medicine, vol. 26, no. 2, 2024, https://doi.org/10.1016/j.gim.2023.101013.