1. Novel NALCN biallelic truncating mutations in siblings with IHPRF1 syndrome. Issue 6 (5th February 2018) Authors: Angius, A.; Cossu, S.; Uva, P.; Oppo, M.; Onano, S.; Persico, I.; Fotia, G.; Atzeni, R.; Cuccuru, G.; Asunis, M.; Cucca, F.; Pruna, D.; Crisponi, L. Journal: Clinical genetics Issue: Volume 93:Issue 6(2018) Page Start: 1245 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗