GL, C., SB, H., SC, Y., JM, M., BJ, O., J, C., . . . HC, M. (2013). Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1. Nature genetics, 45(7), 825. https://doi.org/10.1038/ng.2646
Chicago Style (17th ed.) CitationGL, Carvill, et al. "Targeted Resequencing in Epileptic Encephalopathies Identifies De Novo Mutations in CHD2 and SYNGAP1." Nature Genetics 45, no. 7 (2013): 825. https://doi.org/10.1038/ng.2646.
MLA (9th ed.) CitationGL, Carvill, et al. "Targeted Resequencing in Epileptic Encephalopathies Identifies De Novo Mutations in CHD2 and SYNGAP1." Nature Genetics, vol. 45, no. 7, 2013, p. 825, https://doi.org/10.1038/ng.2646.
Warning: These citations may not always be 100% accurate.