1. Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type. Issue 1 (26th July 2017) Authors: Reinstein, E.; Drasinover, V.; Lotan, R.; Gal‐Tanamy, M.; Bolocan Nachman, I.; Eyal, E.; Jaber, L.; Magal, N.; Shohat, M. Journal: Clinical genetics Issue: Volume 93:Issue 1(2018) Page Start: 160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗