Cite
A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect.
MLA
McEntagart, Meriel, et al. “A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect.” American Journal of Human Genetics, vol. 98, no. 5, May 2016, pp. 981–92. EBSCOhost, https://doi.org/10.1016/j.ajhg.2016.03.018.
APA
McEntagart, M., Williamson, K. A., Rainger, J. K., Wheeler, A., Seawright, A., De Baere, E., Verdin, H., Bergendahl, L. T., Quigley, A., Rainger, J., Dixit, A., Sarkar, A., López Laso, E., Sanchez-Carpintero, R., Barrio, J., Bitoun, P., Prescott, T., Riise, R., McKee, S., … FitzPatrick, D. R. (2016). A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect. American Journal of Human Genetics, 98(5), 981–992. https://doi.org/10.1016/j.ajhg.2016.03.018
Chicago
McEntagart, Meriel, Kathleen A Williamson, Jacqueline K Rainger, Ann Wheeler, Anne Seawright, Elfride De Baere, Hannah Verdin, et al. 2016. “A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect.” American Journal of Human Genetics 98 (5): 981–92. doi:10.1016/j.ajhg.2016.03.018.