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-Reference-Cited by-同舟云学术

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

Published:2020-06-19 Issue:1 Volume:47 Page:26-42
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathol. Appl. Neurobiol.

Author:

Kurzawa‐Akanbi M.¹²^ORCID,Keogh M.¹³⁴,Tsefou E.²,Ramsay L.⁵⁶,Johnson M.⁵,Keers S.⁵,WSA Ochieng L.²,McNair A.²,Singh P.²,Khan A.³,Pyle A.¹,Hudson G.¹,Ince P. G.⁶,Attems J.⁷,Burn J.¹⁸,Chinnery P. F.¹⁴,Morris C. M.²⁵

Affiliation:

1. Biosciences InstituteNewcastle UniversityInternational Centre for Life Newcastle upon Tyne UK

2. Wolfson Building Newcastle University Newcastle upon Tyne UK

3. Department of Neurology Royal Victoria Infirmary Newcastle upon Tyne UK

4. MRC Mitochondrial Biology Unit Department of Clinical Neurosciences Cambridge Biomedical CampusCambridge University Cambridge UK

5. Newcastle Brain Tissue ResourceTranslational and Clinical Research InstituteNewcastle University Newcastle upon Tyne UK

6. Academic Unit of Pathology Royal Hallamshire Hospital Sheffield UK

7. Cellular Pathology Royal Victoria InfirmaryNewcastle upon Tyne Hospitals NHS Foundation Trust Newcastle upon Tyne UK

8. Northern Genetics Service Newcastle upon Tyne Hospitals NHS Foundation TrustInternational Centre for Life Newcastle upon Tyne UK

Publisher

Wiley

Subject

Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/nan.12634

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