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Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
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http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_6/w
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Title
Clinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation
has manifestation of work
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_6/101093brainawn274/m/web
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_6/101093brainawn274/m/print
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http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_6/101093brainawn274/authorship/5
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_6/101093brainawn274/authorship/4
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_6/101093brainawn274/authorship/6
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_6/101093brainawn274/authorship/1
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_6/101093brainawn274/authorship/7
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_6/101093brainawn274/authorship/2
http://hub.abes.fr/oup/periodical/brainj/2009/volume_132/issue_6/101093brainawn274/authorship/3
Author
Vuillaume Isabelle
Chinnery P F
Batey Stephanie
Devos D.
Destée A.
Tchofo P. Jissendi
Burn J.
article type
letter
publisher identifier
awn274
is part of this journal
Brain
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