Cite
HARVARD Citation
Lin, B. et al. (2021). ALS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein import. Human molecular genetics. 30 (13), pp. 1230-1246. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Lin, B. et al. (2021). ALS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein import. Human molecular genetics. 30 (13), pp. 1230-1246. [Online].