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J. R. McNally, M. R. Mehlenbacher, S. Luscieti, G. L. Smith, A. A. Reutovich, P. Maura, P. Arosio, F. Bou-Abdallah: Mutant L-chain ferritins that cause neuroferritinopathy alter ferritin functionality and iron permeability. In: Metallomics : integrated biometal science. Band 11, Nummer 10, Oktober 2019, S. 1635–1647, doi:10.1039/c9mt00154a, PMID 31513212, PMC 6800815 (freier Volltext).
nih.gov
ncbi.nlm.nih.gov
Patrick F. Chinnery: Neuroferritinopathy. In: GeneReviews®. University of Washington, Seattle, Seattle WA 1993, PMID 20301320 (nih.gov [abgerufen am 8. Dezember 2019]).
A. R. Curtis, C. Fey, C. M. Morris, L. A. Bindoff, P. G. Ince, P. F. Chinnery, A. Coulthard, M. J. Jackson, A. P. Jackson, D. P. McHale, D. Hay, W. A. Barker, A. F. Markham, D. Bates, A. Curtis, J. Burn: Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease. In: Nature genetics. Band 28, Nummer 4, August 2001, S. 350–354, doi:10.1038/ng571, PMID 11438811.
N. Kumar, P. Rizek, M. Jog: Neuroferritinopathy: Pathophysiology, Presentation, Differential Diagnoses and Management. In: Tremor and other hyperkinetic movements. Band 6, 2016, S. 355, doi:10.7916/D8KK9BHF, PMID 27022507, PMC 4795517 (freier Volltext) (Review).
S. H. Yoon, N. Y. Kim, Y. J. Kim, C. H. Lyoo: Novel Ferritin Light Chain Gene Mutation in a Korean Patient with Neuroferritinopathy. In: Journal of movement disorders. Band 12, Nummer 1, 01 2019, S. 63–65, doi:10.14802/jmd.18062, PMID 30732435, PMC 6369382 (freier Volltext).
J. R. McNally, M. R. Mehlenbacher, S. Luscieti, G. L. Smith, A. A. Reutovich, P. Maura, P. Arosio, F. Bou-Abdallah: Mutant L-chain ferritins that cause neuroferritinopathy alter ferritin functionality and iron permeability. In: Metallomics : integrated biometal science. Band 11, Nummer 10, Oktober 2019, S. 1635–1647, doi:10.1039/c9mt00154a, PMID 31513212, PMC 6800815 (freier Volltext).
