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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.
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MLA
Naesens, Leslie, et al. “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.” 25th Annual Congress of the Belgian Society of Internal Medicine, Abstracts, 2021.
APA
Naesens, L., Nemegeer, J., Roelens, F., Vallaeys, L., Meuwissen, M., Janssens, K., … Haerynck, F. (2021). 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. 25th Annual Congress of the Belgian Society of Internal Medicine, Abstracts. Presented at the 25th Annual Congress of the Belgian Society of Internal Medicine, Brussels, Belgium.
Chicago author-date
Naesens, Leslie, Josephine Nemegeer, Filip Roelens, Lore Vallaeys, Marije Meuwissen, Katrien Janssens, Patrick Verloo, et al. 2021. “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.” In 25th Annual Congress of the Belgian Society of Internal Medicine, Abstracts.
Chicago author-date (all authors)
Naesens, Leslie, Josephine Nemegeer, Filip Roelens, Lore Vallaeys, Marije Meuwissen, Katrien Janssens, Patrick Verloo, Benson Ogunjimi, Dimitri Hemelsoet, Program for Undiagnosed Rare Diseases (UD-PrOZA), Levi Hoste, Lisa Roels, Marieke De Bruyne, Elfride De Baere, Jo Van Dorpe, Amélie Dendooven, Anne Sieben, Gillian Rice, Tessa Kerre, Rudi Beyaert, Carolina Uggenti, Yanick Crow, Simon Tavernier, Jonathan Maelfait, and Filomeen Haerynck. 2021. “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.” In 25th Annual Congress of the Belgian Society of Internal Medicine, Abstracts.
Vancouver
1.
Naesens L, Nemegeer J, Roelens F, Vallaeys L, Meuwissen M, Janssens K, et al. 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. In: 25th Annual Congress of the Belgian Society of Internal Medicine, Abstracts. 2021.
IEEE
[1]
L. Naesens et al., “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,” in 25th Annual Congress of the Belgian Society of Internal Medicine, Abstracts, Brussels, Belgium, 2021.
@inproceedings{8732651,
  author       = {{Naesens, Leslie and Nemegeer, Josephine and Roelens, Filip and Vallaeys, Lore and Meuwissen, Marije and Janssens, Katrien and Verloo, Patrick and Ogunjimi, Benson and Hemelsoet, Dimitri and (UD-PrOZA), Program for Undiagnosed Rare Diseases and Hoste, Levi and Roels, Lisa and De Bruyne, Marieke and De Baere, Elfride and Van Dorpe, Jo and Dendooven, Amélie and Sieben, Anne and Rice, Gillian and Kerre, Tessa and Beyaert, Rudi and Uggenti, Carolina and Crow, Yanick and Tavernier, Simon and Maelfait, Jonathan and Haerynck, Filomeen}},
  booktitle    = {{25th Annual Congress of the Belgian Society of Internal Medicine, Abstracts}},
  language     = {{eng}},
  location     = {{Brussels, Belgium}},
  title        = {{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}},
  year         = {{2021}},
}