1. THU0002 Novel pathogenic stop codon mutation in the nf-Κb p65 subunit (RELA) associated with both behÇet's disease like syndrome and neuromyelitis optica in an irish family. (12th June 2018) Authors: Adeeb, F.; Dorris, E.R.; Tariq, S.; Ng, W.L.; Stack, A.G.; Wilson, A.G.; Fraser, A.D. Journal: Annals of the rheumatic diseases Issue: Volume 77(2018)Supplement 2 Page Start: 230 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗