Frühmesser, A., Blake, J., Haberlandt, E., Baying, B., Raeder, B., Runz, H., . . . Kotzot, D. (2013). Disruption of EXOC6B in a patient with developmental delay, epilepsy, and a de novo balanced t(2;8) translocation. European Journal of Human Genetics, 21(10), 1177. https://doi.org/10.1038/ejhg.2013.18
Chicago Style (17th ed.) CitationFrühmesser, Anne, et al. "Disruption of EXOC6B in a Patient with Developmental Delay, Epilepsy, and a De Novo Balanced T(2;8) Translocation." European Journal of Human Genetics 21, no. 10 (2013): 1177. https://doi.org/10.1038/ejhg.2013.18.
MLA (9th ed.) CitationFrühmesser, Anne, et al. "Disruption of EXOC6B in a Patient with Developmental Delay, Epilepsy, and a De Novo Balanced T(2;8) Translocation." European Journal of Human Genetics, vol. 21, no. 10, 2013, p. 1177, https://doi.org/10.1038/ejhg.2013.18.