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Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation

Detalles Bibliográficos
Autores principales:	Devos, David, Tchofo, P. Jissendi, Vuillaume, Isabelle, Destée, Alain, Batey, Stephanie, Burn, John, Chinnery, Patrick F.
Formato:	Texto
Lenguaje:	English
Publicado:	Oxford University Press 2009
Materias:	Letters to the Editor
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2685918/ https://www.ncbi.nlm.nih.gov/pubmed/18854324 http://dx.doi.org/10.1093/brain/awn274

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