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Neuroferritinopathy: From ferritin structure modification to pathogenetic mechanism
Neuroferritinopathy is a rare, late-onset, dominantly inherited movement disorder caused by mutations in L-ferritin gene. It is characterized by iron and ferritin aggregate accumulation in brain, normal or low serum ferritin levels and high variable clinical feature. To date, nine causative mutation...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Academic Press
2015
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4642653/ https://www.ncbi.nlm.nih.gov/pubmed/25772441 http://dx.doi.org/10.1016/j.nbd.2015.02.007 |