APA (7th ed.) Citation

D, M., M, J., N, J., H, A., S, D., H, M., . . . B, D. (2024). Genetic investigation of patients with autosomal recessive ataxia and identification of two novel variants in the SQSTM1 and SYNE1 genes. Human genome variation, 11(1), 35. https://doi.org/10.1038/s41439-024-00292-x

Chicago Style (17th ed.) Citation

D, Mokhtari, et al. "Genetic Investigation of Patients with Autosomal Recessive Ataxia and Identification of Two Novel Variants in the SQSTM1 and SYNE1 Genes." Human Genome Variation 11, no. 1 (2024): 35. https://doi.org/10.1038/s41439-024-00292-x.

MLA (9th ed.) Citation

D, Mokhtari, et al. "Genetic Investigation of Patients with Autosomal Recessive Ataxia and Identification of Two Novel Variants in the SQSTM1 and SYNE1 Genes." Human Genome Variation, vol. 11, no. 1, 2024, p. 35, https://doi.org/10.1038/s41439-024-00292-x.