APA (7th ed.) Citation

AE, F., E, R., R, T., K, M., P, B., G, J., . . . MP, K. (2016). Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy. BMC medical genetics, 17(1), 34. https://doi.org/10.1186/s12881-016-0294-2

Chicago Style (17th ed.) Citation

AE, Fry, et al. "Pathogenic Copy Number Variants and SCN1A Mutations in Patients with Intellectual Disability and Childhood-onset Epilepsy." BMC Medical Genetics 17, no. 1 (2016): 34. https://doi.org/10.1186/s12881-016-0294-2.

MLA (9th ed.) Citation

AE, Fry, et al. "Pathogenic Copy Number Variants and SCN1A Mutations in Patients with Intellectual Disability and Childhood-onset Epilepsy." BMC Medical Genetics, vol. 17, no. 1, 2016, p. 34, https://doi.org/10.1186/s12881-016-0294-2.