000			02069 a2200649 4500
005			20250516060720.0
264		0	_c20120713
008			201207s 0 0 eng d
022			_a1872-8278
024	7		_a10.1016/j.mito.2011.09.007 _2doi
040			_aNLM _beng _cNLM
100	1		_aGalmiche, Louise
245	0	0	_aToward genotype phenotype correlations in GFM1 mutations. _h[electronic resource]
260			_bMitochondrion _cMar 2012
300			_a242-7 p. _bdigital
500			_aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAmino Acid Sequence
650	0	4	_aAmino Acid Substitution
650	0	4	_aBrain _xdiagnostic imaging
650	0	4	_aBrain Damage, Chronic _xgenetics
650	0	4	_aFemale
650	0	4	_aGenetic Association Studies
650	0	4	_aHumans
650	0	4	_aInfant
650	0	4	_aInfant, Newborn
650	0	4	_aLiver Failure _xgenetics
650	0	4	_aMagnetic Resonance Imaging
650	0	4	_aMale
650	0	4	_aMitochondrial Diseases _xgenetics
650	0	4	_aMitochondrial Proteins _xgenetics
650	0	4	_aModels, Molecular
650	0	4	_aMolecular Dynamics Simulation
650	0	4	_aMolecular Sequence Data
650	0	4	_aMutant Proteins _xgenetics
650	0	4	_aMutation, Missense
650	0	4	_aPeptide Elongation Factor G _xgenetics
650	0	4	_aPregnancy
650	0	4	_aRadiography
650	0	4	_aSequence Analysis, DNA
700	1		_aSerre, Valérie
700	1		_aBeinat, Marine
700	1		_aZossou, Raïssa
700	1		_aAssouline, Zahra
700	1		_aLebre, Anne-Sophie
700	1		_aChretien, Florence
700	1		_aShenhav, Ruthie
700	1		_aZeharia, Avraham
700	1		_aSaada, Ann
700	1		_aVedrenne, Vanessa
700	1		_aBoddaert, Nathalie
700	1		_ade Lonlay, Pascale
700	1		_aRio, Marlène
700	1		_aMunnich, Arnold
700	1		_aRötig, Agnès
773	0		_tMitochondrion _gvol. 12 _gno. 2 _gp. 242-7
856	4	0	_uhttps://doi.org/10.1016/j.mito.2011.09.007 _zAvailable from publisher's website
999			_c21220231 _d21220231