Cite

    Paciorkowski, A. R., McDaniel, S. S., Jansen, L. A., Tully, H., Tuttle, E., Ghoneim, D. H., Tupal, S., Gunter, S. A., Vasta, V., Zhang, Q., Tran, T., Liu, Y. B., Ozelius, L. J., Brashear, A., Sweadner, K. J., Dobyns, W. B., & Hahn, S. (n.d.). novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly. Epilepsia, 56, 422–430. http://access.bl.uk/ark:/81055/vdc_100042690699.0x000060