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APA Citation
Lin, B. C., Phung, T. H., Higgins, N. R., Greenslade, J. E., Prado, M. A., Finley, D., Karbowski, M., Polster, B. M., & Monteiro, M. J. (2021). aLS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein import. Human molecular genetics, 30(13), 1230–1246. http://access.bl.uk/ark:/81055/vdc_100133386464.0x000014