000 01462 a2200409 4500
005 20250516055717.0
264 0 _c20120521
008 201205s 0 0 eng d
022 _a1531-8257
024 7 _a10.1002/mds.23956
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aMéneret, Aurélie
245 0 0 _aGeneralized dystonia, athetosis, and parkinsonism associated with FOXG1 mutation.
_h[electronic resource]
260 _bMovement disorders : official journal of the Movement Disorder Society
_cJan 2012
300 _a160-1 p.
_bdigital
500 _aPublication Type: Case Reports; Letter
650 0 4 _aAdult
650 0 4 _aAthetosis
_xcomplications
650 0 4 _aBrain
_xpathology
650 0 4 _aDystonic Disorders
_xcomplications
650 0 4 _aFemale
650 0 4 _aForkhead Transcription Factors
_xgenetics
650 0 4 _aHumans
650 0 4 _aMagnetic Resonance Imaging
650 0 4 _aMutation
_xgenetics
650 0 4 _aNerve Tissue Proteins
_xgenetics
650 0 4 _aParkinsonian Disorders
_xcomplications
700 1 _aMignot, Cyril
700 1 _aAn, Isabelle
700 1 _aHabert, Marie-Odile
700 1 _aJacquette, Aurélia
700 1 _aVidailhet, Marie
700 1 _aBienvenu, Thierry
700 1 _aRoze, Emmanuel
773 0 _tMovement disorders : official journal of the Movement Disorder Society
_gvol. 27
_gno. 1
_gp. 160-1
856 4 0 _uhttps://doi.org/10.1002/mds.23956
_zAvailable from publisher's website
999 _c21190991
_d21190991