Abnormal iron metabolism and oxidative stress in mice expressing a mutant form of the ferritin light polypeptide gene

Insertional mutations in exon 4 of the ferritin light chain (FTL) gene are associated with hereditary ferritinopathy (HF) or neuroferritinopathy, an autosomal dominant neurodegenerative disease characterized by progressive impairment of motor and cognitive functions. To determine the pathogenic mech...

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Main Authors: Barbeito, Ana G., Garringer, Holly J., Baraibar, Martin A., Gao, Xiaoying, Arredondo, Miguel, Núñez, Marco T., Smith, Mark A., Ghetti, Bernardino, Vidal, Ruben
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2696070/
https://ncbi.nlm.nih.gov/pubmed/19519778
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1471-4159.2009.06028.x
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