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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author Devos, David
Tchofo, P. Jissendi
Vuillaume, Isabelle
Destée, Alain
Batey, Stephanie
Burn, John
Chinnery, Patrick F.
author_facet Devos, David
Tchofo, P. Jissendi
Vuillaume, Isabelle
Destée, Alain
Batey, Stephanie
Burn, John
Chinnery, Patrick F.
author_sort Devos, David
collection PubMed
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spelling pubmed-26859182009-05-26 Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation Devos, David Tchofo, P. Jissendi Vuillaume, Isabelle Destée, Alain Batey, Stephanie Burn, John Chinnery, Patrick F. Brain Letters to the Editor Oxford University Press 2009-06 2008-10-14 /pmc/articles/PMC2685918/ /pubmed/18854324 http://dx.doi.org/10.1093/brain/awn274 Text en © 2008 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Letters to the Editor
Devos, David
Tchofo, P. Jissendi
Vuillaume, Isabelle
Destée, Alain
Batey, Stephanie
Burn, John
Chinnery, Patrick F.
Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
title Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
title_full Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
title_fullStr Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
title_full_unstemmed Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
title_short Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
title_sort clinical features and natural history of neuroferritinopathy caused by the 458dupa ftl mutation
topic Letters to the Editor
url 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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