APA (7th ed.) Citation

LTK, V., HTD, H., HTT, K., NLT, H., LS, V., G, H., & DTT, H. (2021). De novo homozygous variant of the SCN1A gene in a patient with severe Dravet syndrome complicated by acute encephalopathy. Neurogenetics, 22(2), 133. https://doi.org/10.1007/s10048-021-00636-7

Chicago Style (17th ed.) Citation

LTK, Van, Hien HTD, Kieu HTT, Hieu NLT, Vinh LS, Hoa G, and Hang DTT. "De Novo Homozygous Variant of the SCN1A Gene in a Patient with Severe Dravet Syndrome Complicated by Acute Encephalopathy." Neurogenetics 22, no. 2 (2021): 133. https://doi.org/10.1007/s10048-021-00636-7.

MLA (9th ed.) Citation

LTK, Van, et al. "De Novo Homozygous Variant of the SCN1A Gene in a Patient with Severe Dravet Syndrome Complicated by Acute Encephalopathy." Neurogenetics, vol. 22, no. 2, 2021, p. 133, https://doi.org/10.1007/s10048-021-00636-7.