Show 100 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="(UD-PrOZA), Program for Undiagnosed Rare Diseases" or (type any "bookEditor issueEditor" ... Add to list Conference Paper C3 Novel mutations in RNU7-1 weaken secondary RNA structure, induce MCP-1 and CXCL10 in CSF and result in Aicardi-Goutières syndrome with severe end-organ involvement Leslie Naesens (UGent) , Josephine Nemegeer (UGent) , Filip Roelens, Lore Vallaeys, Marije Meuwissen, Katrien Janssens, Patrick Verloo (UGent) , Benson Ogunjimi (UGent) , Dimitri Hemelsoet (UGent) , Program for Undiagnosed Rare Diseases (UD-PrOZA), et al. (2021) 25th Annual Congress of the Belgian Society of Internal Medicine, Abstracts.