1. Clinical variability and female penetrance in X-linked familial FTD/ALS caused by a P506S mutation in UBQLN2. Issue 7 (December 2013) Authors: Vengoechea, Jaime; David, Marjorie P.; Yaghi, Shadi R.; Carpenter, Lori; Rudnicki, Stacy A. Journal: Amyotrophic lateral sclerosis and frontotemporal degeneration Issue: Volume 14:Issue 7/8(2013) Page Start: 615 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗