Maksemous, N.; Smith, R.A.; Sutherland, H.G.; Sampaio, H.; Griffiths, L.R.
Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity. Int. J. Mol. Sci. 2018, 19, 3113.
https://doi.org/10.3390/ijms19103113
AMA Style
Maksemous N, Smith RA, Sutherland HG, Sampaio H, Griffiths LR.
Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity. International Journal of Molecular Sciences. 2018; 19(10):3113.
https://doi.org/10.3390/ijms19103113
Chicago/Turabian Style
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, no. 10: 3113.
https://doi.org/10.3390/ijms19103113
APA Style
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