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Author/Creator Chinnery, P. F.

2. 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
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