1. Novel homozygous missense mutation in GAN associated with Charcot-Marie-Tooth disease type 2 in a large consanguineous family from Israel. Issue 1 (December 2016) Authors: Aharoni, Sharon; Barwick, Katy; Straussberg, Rachel; Harlalka, Gaurav; Nevo, Yoram; Chioza, Barry; McEntagart, Meriel; Mimouni-Bloch, Aviva; Weedon, Michael; Crosby, Andrew Journal: BMC medical genetics Issue: Volume 17:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗