1. Recessive mutations in NDUFA2 cause mitochondrial leukoencephalopathy. Issue 2 (21st December 2017) Authors: Perrier, S.; Gauquelin, L.; Tétreault, M.; Tran, L.T.; Webb, N.; Srour, M.; Mitchell, J.J.; Brunel‐Guitton, C.; Majewski, J.; Long, V.; Keller, S.; Gambello, M.J.; Simons, C.; Vanderver, A.; Bernard, G. Journal: Clinical genetics Issue: Volume 93:Issue 2(2018) Page Start: 396 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Therapies in Aicardi–Goutières syndrome. (January 2014) Authors: Crow, Y. J.; Vanderver, A.; Orcesi, S.; Kuijpers, T. W.; Rice, G. I. Journal: Clinical and experimental immunology Issue: Volume 175:Number 1(2014:Jan.) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗