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Neuroferritinopathy: Pathophysiology, Presentation, Differential Diagnoses and Management
BACKGROUND: Neuroferritinopathy (NF) is a rare autosomal dominant disease caused by mutations in the ferritin light chain 1 (FTL1) gene leading to abnormal excessive iron accumulation in the brain, predominantly in the basal ganglia. METHODS: A literature search was performed on Pubmed, for English-...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Columbia University Libraries/Information Services
2016
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795517/ https://www.ncbi.nlm.nih.gov/pubmed/27022507 http://dx.doi.org/10.7916/D8KK9BHF |