1. ALS/FTD mutations in UBQLN2 are linked to mitochondrial dysfunction through loss-of-function in mitochondrial protein import. Issue 13 (22nd April 2021) Authors: Lin, Brian C; Phung, Trong H; Higgins, Nicole R; Greenslade, Jessie E; Prado, Miguel A; Finley, Daniel; Karbowski, Mariusz; Polster, Brian M; Monteiro, Mervyn J Journal: Human molecular genetics Issue: Volume 30:Issue 13(2021) Page Start: 1230 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗