000 01699 a2200517 4500
005 20250515033154.0
264 0 _c20070202
008 200702s 0 0 eng d
022 _a0885-3185
024 7 _a10.1002/mds.21031
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aBauer, Peter
245 0 0 _aMutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause.
_h[electronic resource]
260 _bMovement disorders : official journal of the Movement Disorder Society
_cOct 2006
300 _a1734-7 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
650 0 4 _aAdolescent
650 0 4 _aAdult
650 0 4 _aAged
650 0 4 _aChild
650 0 4 _aChild, Preschool
650 0 4 _aChorea
_xdiagnosis
650 0 4 _aChromosome Aberrations
650 0 4 _aFemale
650 0 4 _aFinland
650 0 4 _aGenes, Dominant
650 0 4 _aGenotype
650 0 4 _aHumans
650 0 4 _aInfant
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMutation
_xgenetics
650 0 4 _aNuclear Proteins
_xgenetics
650 0 4 _aPolymerase Chain Reaction
650 0 4 _aThyroid Nuclear Factor 1
650 0 4 _aTranscription Factors
_xgenetics
700 1 _aKreuz, Friedmar R
700 1 _aBürk, Katrin
700 1 _aSaft, Carsten
700 1 _aAndrich, Jürgen
700 1 _aHeilemann, Hubert
700 1 _aRiess, Olaf
700 1 _aSchöls, Ludger
773 0 _tMovement disorders : official journal of the Movement Disorder Society
_gvol. 21
_gno. 10
_gp. 1734-7
856 4 0 _uhttps://doi.org/10.1002/mds.21031
_zAvailable from publisher's website
999 _c16421762
_d16421762