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APA Citation
Duis, J., Dean, S., Applegate, C., Harper, A., Xiao, R., He, W., Dollar, J. D., Sun, L. R., Waberski, M. B., Crawford, T. O., Hamosh, A., & Stafstrom, C. E. (n.d.). kIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction. Annals of neurology, 80(4), 633–637. http://access.bl.uk/ark:/81055/vdc_100036756234.0x000013