C, D., O, T., I, G., C, S., D, B., D, G., . . . E, L. (2010). Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome. Journal of medical genetics, 47(6), 404. https://doi.org/10.1136/jmg.2009.074328
Chicago Style (17th ed.) CitationC, Depienne, et al. "Mechanisms for Variable Expressivity of Inherited SCN1A Mutations Causing Dravet Syndrome." Journal of Medical Genetics 47, no. 6 (2010): 404. https://doi.org/10.1136/jmg.2009.074328.
MLA (9th ed.) CitationC, Depienne, et al. "Mechanisms for Variable Expressivity of Inherited SCN1A Mutations Causing Dravet Syndrome." Journal of Medical Genetics, vol. 47, no. 6, 2010, p. 404, https://doi.org/10.1136/jmg.2009.074328.
Warning: These citations may not always be 100% accurate.