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 |