1. Novel B4GALNT1 mutations in a complicated form of hereditary spastic paraplegia. (27th November 2013) Authors: Wakil, S.M.; Monies, D.M.; Ramzan, K.; Hagos, S.; Bastaki, L.; Meyer, B.F.; Bohlega, S. Journal: Clinical genetics Issue: Volume 86:Number 5(2014:Nov.) Page Start: 500 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗