1. Variants in the genes DCTN2, DNAH10, LRIG3, and MYO1A are associated with intermediate Charcot–Marie–Tooth disease in a Norwegian family. (12th October 2015) Authors: Braathen, G. J.; Høyer, H.; Busk, Ø. L.; Tveten, K.; Skjelbred, C. F.; Russell, M. B. Journal: Acta neurologica Scandinavica Issue: Volume 134:Number 1(2016:Jul.) Page Start: 67 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗