000 01102 a2200325 4500
005 20250517035054.0
264 0 _c20150813
008 201508s 0 0 eng d
022 _a1474-4465
024 7 _a10.1016/S1474-4422(15)00096-4
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aIqbal, Zafar
245 0 0 _aCHCHD2 and Parkinson's disease.
_h[electronic resource]
260 _bThe Lancet. Neurology
_cJul 2015
300 _a680-1 p.
_bdigital
500 _aPublication Type: Letter; Comment
650 0 4 _aFemale
650 0 4 _aGenetic Linkage
_xgenetics
650 0 4 _aGenome-Wide Association Study
_xmethods
650 0 4 _aHumans
650 0 4 _aMale
650 0 4 _aMitochondrial Proteins
_xgenetics
650 0 4 _aMutation, Missense
_xgenetics
650 0 4 _aParkinsonian Disorders
_xgenetics
650 0 4 _aSequence Analysis, DNA
_xmethods
650 0 4 _aTranscription Factors
_xgenetics
700 1 _aToft, Mathias
773 0 _tThe Lancet. Neurology
_gvol. 14
_gno. 7
_gp. 680-1
856 4 0 _uhttps://doi.org/10.1016/S1474-4422(15)00096-4
_zAvailable from publisher's website
999 _c24974776
_d24974776