EL, H., KJ, S., Y, H., F, G., S, N., B, d. V., . . . DB, G. (2012). De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. Nature genetics, 44(9), 1030. https://doi.org/10.1038/ng.2358
Chicago Style (17th ed.) CitationEL, Heinzen, et al. "De Novo Mutations in ATP1A3 Cause Alternating Hemiplegia of Childhood." Nature Genetics 44, no. 9 (2012): 1030. https://doi.org/10.1038/ng.2358.
MLA (9th ed.) CitationEL, Heinzen, et al. "De Novo Mutations in ATP1A3 Cause Alternating Hemiplegia of Childhood." Nature Genetics, vol. 44, no. 9, 2012, p. 1030, https://doi.org/10.1038/ng.2358.
Warning: These citations may not always be 100% accurate.
