APA (7th ed.) Citation

R, U., K, M., GD, E., E, S., L, C., NAL, C., . . . S, B. (2020). DPH1 syndrome: Two novel variants and structural and functional analyses of seven missense variants identified in syndromic patients. European journal of human genetics : EJHG, 28(1), 64. https://doi.org/10.1038/s41431-019-0374-9

Chicago Style (17th ed.) Citation

R, Urreizti, et al. "DPH1 Syndrome: Two Novel Variants and Structural and Functional Analyses of Seven Missense Variants Identified in Syndromic Patients." European Journal of Human Genetics : EJHG 28, no. 1 (2020): 64. https://doi.org/10.1038/s41431-019-0374-9.

MLA (9th ed.) Citation

R, Urreizti, et al. "DPH1 Syndrome: Two Novel Variants and Structural and Functional Analyses of Seven Missense Variants Identified in Syndromic Patients." European Journal of Human Genetics : EJHG, vol. 28, no. 1, 2020, p. 64, https://doi.org/10.1038/s41431-019-0374-9.