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APA Citation
Hitomi, Y., Heinzen, E. L., Donatello, S., Dahl, H., Damiano, J. A., McMahon, J. M., Berkovic, S. F., Scheffer, I. E., Legros, B., Rai, M., Weckhuysen, S., Suls, A., De, P., Pandolfo, M., Goldstein, D. B., Van, P., & Depondt, C. (n.d.). mutations in TNK2 in severe autosomal recessive infantile onset epilepsy. Annals of neurology, 74(3), 496–501. http://access.bl.uk/ark:/81055/vdc_100024743242.0x000025