APA (7th ed.) Citation

T, S., F, P., A, P., B, K., D, S., A, A., . . . J, G. (2018). MED13L-related intellectual disability: Involvement of missense variants and delineation of the phenotype. Neurogenetics, 19(2), 93. https://doi.org/10.1007/s10048-018-0541-0

Chicago Style (17th ed.) Citation

T, Smol, et al. "MED13L-related Intellectual Disability: Involvement of Missense Variants and Delineation of the Phenotype." Neurogenetics 19, no. 2 (2018): 93. https://doi.org/10.1007/s10048-018-0541-0.

MLA (9th ed.) Citation

T, Smol, et al. "MED13L-related Intellectual Disability: Involvement of Missense Variants and Delineation of the Phenotype." Neurogenetics, vol. 19, no. 2, 2018, p. 93, https://doi.org/10.1007/s10048-018-0541-0.