Hoed, J. d., de Boer, E., Voisin, N., Dingemans, A. J. M., Guex, N., Wiel, L., . . . Orec, L. (2021). Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction. The American journal of human genetics, 108(2), . https://doi.org/10.1016/j.ajhg.2021.01.007
Chicago Style (17th ed.) CitationHoed, Joery den, et al. "Mutation-specific Pathophysiological Mechanisms Define Different Neurodevelopmental Disorders Associated with SATB1 Dysfunction." The American Journal of Human Genetics 108, no. 2 (2021). https://doi.org/10.1016/j.ajhg.2021.01.007.
MLA (9th ed.) CitationHoed, Joery den, et al. "Mutation-specific Pathophysiological Mechanisms Define Different Neurodevelopmental Disorders Associated with SATB1 Dysfunction." The American Journal of Human Genetics, vol. 108, no. 2, 2021, https://doi.org/10.1016/j.ajhg.2021.01.007.