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APA Citation
Helman, G., Takanohashi, A., Hagemann, T. L., Perng, M. D., Walkiewicz, M., Woidill, S., Sase, S., Cross, Z., Du, Y., Zhao, L., Waldman, A., Haake, B. C., Fatemi, A., Brenner, M., Sherbini, O., Messing, A., Vanderver, A., & Simons, C. (2020). type II Alexander disease caused by splicing errors and aberrant overexpression of an uncharacterized GFAP isoform. Human mutation, 41(6), 1131–1137. http://access.bl.uk/ark:/81055/vdc_100102668315.0x000039