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Lin BC, Phung TH, Higgins NR, et al. ALS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein import. Hum Mol Genet. 2021;30(13):1230-1246doi: 10.1093/hmg/ddab116.
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. https://doi.org/10.1093/hmg/ddab116
Lin, Brian C, et al. "ALS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein import." Human molecular genetics vol. 30,13 (2021): 1230-1246. doi: https://doi.org/10.1093/hmg/ddab116
Lin BC, Phung TH, Higgins NR, Greenslade JE, Prado MA, Finley D, Karbowski M, Polster BM, Monteiro MJ. ALS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein import. Hum Mol Genet. 2021 Jun 17;30(13):1230-1246. doi: 10.1093/hmg/ddab116. PMID: 33891006; PMCID: PMC8212775.
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