Cite
Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity.
MLA
Maksemous, Neven, et al. “Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity.” International Journal of Molecular Sciences, vol. 19, no. 10, Oct. 2018, p. 3113. EBSCOhost, https://doi.org/10.3390/ijms19103113.
APA
Maksemous, N., Smith, R. A., Sutherland, H. G., Sampaio, H., & Griffiths, L. R. (2018). Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity. International Journal of Molecular Sciences, 19(10), 3113. https://doi.org/10.3390/ijms19103113
Chicago
Maksemous, Neven, Robert A. Smith, Heidi G. Sutherland, Hugo Sampaio, and Lyn R. Griffiths. 2018. “Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity.” International Journal of Molecular Sciences 19 (10): 3113. doi:10.3390/ijms19103113.