Associated Papers
Novel mutations and molecular pathways identified in patients with brain iron accumulation disorders.
Si L et al.
Neurogenetics, 2023
Pathogenic mechanism and modeling of neuroferritinopathy.
Cozzi A et al.
Cellular and Molecular Life Sciences : Cmls, 2021
L-Ferritin: One Gene, Five Diseases; from Hereditary Hyperferritinemia to Hypoferritinemia-Report of New Cases.
Cadenas B et al.
Pharmaceuticals (basel, Switzerland), 2019
30678075 (PubMed )
Supplement: pharmaceuticals-12-00017-s001.pdf
Iron, Ferritin, Hereditary Ferritinopathy, and Neurodegeneration.
Muhoberac BB et al.
Frontiers in Neuroscience, 2019
FTL mutation in a Chinese pedigree with neuroferritinopathy.
Ni W et al.
Neurology. Genetics, 2016
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