000			01950 a2200685 4500
005			20250515223729.0
264		0	_c20100602
008			201006s 0 0 eng d
022			_a1526-632X
024	7		_a10.1212/WNL.0b013e3181df099f _2doi
040			_aNLM _beng _cNLM
100	1		_aFratter, C
245	0	0	_aThe clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEO. _h[electronic resource]
260			_bNeurology _cMay 2010
300			_a1619-26 p. _bdigital
500			_aPublication Type: Journal Article
650	0	4	_aAdolescent
650	0	4	_aAdult
650	0	4	_aAge of Onset
650	0	4	_aAged
650	0	4	_aChild
650	0	4	_aDNA Helicases _xgenetics
650	0	4	_aDNA, Mitochondrial _xgenetics
650	0	4	_aFemale
650	0	4	_aGenetic Association Studies
650	0	4	_aHumans
650	0	4	_aMale
650	0	4	_aMiddle Aged
650	0	4	_aMitochondria, Muscle _xgenetics
650	0	4	_aMitochondrial Proteins
650	0	4	_aMuscle, Skeletal _xpathology
650	0	4	_aMutation _xgenetics
650	0	4	_aOculomotor Muscles _xpathology
650	0	4	_aOphthalmoplegia, Chronic Progressive External _xgenetics
650	0	4	_aPhenotype
700	1		_aGorman, G S
700	1		_aStewart, J D
700	1		_aBuddles, M
700	1		_aSmith, C
700	1		_aEvans, J
700	1		_aSeller, A
700	1		_aPoulton, J
700	1		_aRoberts, M
700	1		_aHanna, M G
700	1		_aRahman, S
700	1		_aOmer, S E
700	1		_aKlopstock, T
700	1		_aSchoser, B
700	1		_aKornblum, C
700	1		_aCzermin, B
700	1		_aLecky, B
700	1		_aBlakely, E L
700	1		_aCraig, K
700	1		_aChinnery, P F
700	1		_aTurnbull, D M
700	1		_aHorvath, R
700	1		_aTaylor, R W
773	0		_tNeurology _gvol. 74 _gno. 20 _gp. 1619-26
856	4	0	_uhttps://doi.org/10.1212/WNL.0b013e3181df099f _zAvailable from publisher's website
999			_c19833374 _d19833374