Abnormal iron metabolism in fibroblasts from a patient with the neurodegenerative disease hereditary ferritinopathy

BACKGROUND: Nucleotide duplications in exon 4 of the ferritin light polypeptide (FTL) gene cause the autosomal dominant neurodegenerative disease neuroferritinopathy or hereditary ferritinopathy (HF). Pathologic examination of patients with HF has shown abnormal ferritin and iron accumulation in neu...

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Detalles Bibliográficos
Autores principales: Barbeito, Ana G, Levade, Thierry, Delisle, Marie B, Ghetti, Bernardino, Vidal, Ruben
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993710/
https://www.ncbi.nlm.nih.gov/pubmed/21067605
http://dx.doi.org/10.1186/1750-1326-5-50

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2993710/
https://www.ncbi.nlm.nih.gov/pubmed/21067605
http://dx.doi.org/10.1186/1750-1326-5-50

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