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APA Citation
O'Grady, G. L., Verschuuren, C., Yuen, M., Webster, R., Menezes, M., Fock, J. M., Pride, N., Best, H. A., Benavides Damm, T., Turner, C., Lek, M., Engel, A. G., North, K. N., Clarke, N. F., MacArthur, D. G., Kamsteeg, E., & Cooper, S. T. (2016). variants in SLC18A3, vesicular acetylcholine transporter, cause congenital myasthenic syndrome. Neurology, 87, . http://access.bl.uk/ark:/81055/vdc_100041981378.0x000055