APA (7th ed.) Citation

HC, M., GE, K., AT, P., Y, M., GL, C., E, M., . . . JC, T. (2014). Clinical whole-genome sequencing in severe early-onset epilepsy reveals new genes and improves molecular diagnosis. Human molecular genetics, 23(12), 3200. https://doi.org/10.1093/hmg/ddu030

Chicago Style (17th ed.) Citation

HC, Martin, et al. "Clinical Whole-genome Sequencing in Severe Early-onset Epilepsy Reveals New Genes and Improves Molecular Diagnosis." Human Molecular Genetics 23, no. 12 (2014): 3200. https://doi.org/10.1093/hmg/ddu030.

MLA (9th ed.) Citation

HC, Martin, et al. "Clinical Whole-genome Sequencing in Severe Early-onset Epilepsy Reveals New Genes and Improves Molecular Diagnosis." Human Molecular Genetics, vol. 23, no. 12, 2014, p. 3200, https://doi.org/10.1093/hmg/ddu030.