000 01397 a2200421 4500
005 20250516092302.0
264 0 _c20130620
008 201306s 0 0 eng d
022 _a1432-1459
024 7 _a10.1007/s00415-012-6535-1
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aSynofzik, Matthis
245 0 0 _aPOLG and PEO1 (Twinkle) mutations are infrequent in PSP-like atypical parkinsonism: a preliminary screening study.
_h[electronic resource]
260 _bJournal of neurology
_cOct 2012
300 _a2232-3 p.
_bdigital
500 _aPublication Type: Letter; Research Support, Non-U.S. Gov't
650 0 4 _aAged
650 0 4 _aDNA Helicases
_xgenetics
650 0 4 _aDNA Polymerase gamma
650 0 4 _aDNA-Directed DNA Polymerase
_xgenetics
650 0 4 _aFemale
650 0 4 _aGenetic Testing
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMiddle Aged
650 0 4 _aMitochondrial Proteins
_xgenetics
650 0 4 _aMutation
650 0 4 _aParkinsonian Disorders
_xgenetics
650 0 4 _aPhenotype
700 1 _aSchicks, Julia
700 1 _aSrulijes, Karin
700 1 _aSchulte, Claudia
700 1 _aSchiele, Franziska
700 1 _aBerg, Daniela
700 1 _aSchöls, Ludger
773 0 _tJournal of neurology
_gvol. 259
_gno. 10
_gp. 2232-3
856 4 0 _uhttps://doi.org/10.1007/s00415-012-6535-1
_zAvailable from publisher's website
999 _c21776578
_d21776578