000			02087 a2200637 4500
005			20250515013617.0
264		0	_c20060425
008			200604s 0 0 eng d
022			_a0364-5134
024	7		_a10.1002/ana.20797 _2doi
040			_aNLM _beng _cNLM
100	1		_aZüchner, Stephan
245	0	0	_aAxonal neuropathy with optic atrophy is caused by mutations in mitofusin 2. _h[electronic resource]
260			_bAnnals of neurology _cFeb 2006
300			_a276-81 p. _bdigital
500			_aPublication Type: Comparative Study; 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	_aAge of Onset
650	0	4	_aCharcot-Marie-Tooth Disease _xcomplications
650	0	4	_aChild
650	0	4	_aDNA Mutational Analysis _xmethods
650	0	4	_aFamily Health
650	0	4	_aGTP Phosphohydrolases
650	0	4	_aGenetic Predisposition to Disease _xgenetics
650	0	4	_aHumans
650	0	4	_aMembrane Proteins _xgenetics
650	0	4	_aMiddle Aged
650	0	4	_aMitochondrial Proteins _xgenetics
650	0	4	_aModels, Biological
650	0	4	_aMutation
650	0	4	_aNeural Conduction _xphysiology
650	0	4	_aOptic Atrophy _xetiology
650	0	4	_aPedigree
650	0	4	_aVisual Acuity _xphysiology
700	1		_aDe Jonghe, Peter
700	1		_aJordanova, Albena
700	1		_aClaeys, Kristl G
700	1		_aGuergueltcheva, Velina
700	1		_aCherninkova, Sylvia
700	1		_aHamilton, Steven R
700	1		_aVan Stavern, Greg
700	1		_aKrajewski, Karen M
700	1		_aStajich, Jeffery
700	1		_aTournev, Ivajlo
700	1		_aVerhoeven, Kristien
700	1		_aLangerhorst, Christine T
700	1		_ade Visser, Marianne
700	1		_aBaas, Frank
700	1		_aBird, Thomas
700	1		_aTimmerman, Vincent
700	1		_aShy, Michael
700	1		_aVance, Jeffery M
773	0		_tAnnals of neurology _gvol. 59 _gno. 2 _gp. 276-81
856	4	0	_uhttps://doi.org/10.1002/ana.20797 _zAvailable from publisher's website
999			_c16052098 _d16052098