1. Neuropathological and biochemical investigation of Hereditary Ferritinopathy cases with ferritin light chain mutation: Prominent protein aggregation in the absence of major mitochondrial or oxidative stress. (19th June 2020) Authors: Kurzawa‐Akanbi, M.; Keogh, M.; Tsefou, E.; Ramsay, L.; Johnson, M.; Keers, S.; WSA Ochieng, L.; McNair, A.; Singh, P.; Khan, A.; Pyle, A.; Hudson, G.; Ince, P. G.; Attems, J.; Burn, J.; Chinnery, P. F.; Morris, C. M. Journal: Neuropathology & applied neurobiology Issue: Volume 47:Number 1(2021) Page Start: 26 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗