1. Additional de novo missense genetic variants in NALCN associated with CLIFAHDD syndrome. Issue 6 (30th January 2017) Authors: Vivero, M.; Cho, M.T.; Begtrup, A.; Wentzensen, I.M.; Walsh, L.; Payne, K.; Zarate, Y.A.; Bosanko, K.; Schaefer, G.B.; DeBrosse, S.; Pollack, L.; Mason, K.; Retterer, K.; DeWard, S.; Juusola, J.; Chung, W.K. Journal: Clinical genetics Issue: Volume 91:Issue 6(2017) Page Start: 929 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗