000 01260 a2200397 4500
005 20250515141223.0
264 0 _c20090630
008 200906s 0 0 eng d
022 _a1460-2156
024 7 _a10.1093/brain/awn274
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aDevos, David
245 0 0 _aClinical features and natural history of neuroferritinopathy caused by the 458dupA FTL mutation.
_h[electronic resource]
260 _bBrain : a journal of neurology
_cJun 2009
300 _ae109 p.
_bdigital
500 _aPublication Type: Comment; Letter
650 0 4 _aAdult
650 0 4 _aApoferritins
_xgenetics
650 0 4 _aDisease Progression
650 0 4 _aDystonic Disorders
_xgenetics
650 0 4 _aFemale
650 0 4 _aFerritins
_xmetabolism
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMutation
650 0 4 _aPhenotype
650 0 4 _aYoung Adult
700 1 _aTchofo, P Jissendi
700 1 _aVuillaume, Isabelle
700 1 _aDestée, Alain
700 1 _aBatey, Stephanie
700 1 _aBurn, John
700 1 _aChinnery, Patrick F
773 0 _tBrain : a journal of neurology
_gvol. 132
_gno. Pt 6
_gp. e109
856 4 0 _uhttps://doi.org/10.1093/brain/awn274
_zAvailable from publisher's website
999 _c18319055
_d18319055