000			01918 a2200577 4500
005			20250513185214.0
264		0	_c19990805
008			199908s 0 0 eng d
022			_a0021-9738
024	7		_a10.1172/JCI6184 _2doi
040			_aNLM _beng _cNLM
100	1		_aProcaccio, V
245	0	0	_aNuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts. _h[electronic resource]
260			_bThe Journal of clinical investigation _cJul 1999
300			_a83-92 p. _bdigital
500			_aPublication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAcidosis, Lactic _xcongenital
650	0	4	_aCell Nucleus _xchemistry
650	0	4	_aCells, Cultured
650	0	4	_aDNA _xgenetics
650	0	4	_aDNA Mutational Analysis
650	0	4	_aDNA, Complementary _xgenetics
650	0	4	_aDNA, Mitochondrial _xgenetics
650	0	4	_aElectron Transport
650	0	4	_aFatal Outcome
650	0	4	_aFibroblasts _xenzymology
650	0	4	_aGenetic Complementation Test
650	0	4	_aGenetic Heterogeneity
650	0	4	_aHumans
650	0	4	_aHybrid Cells
650	0	4	_aInfant
650	0	4	_aInfant, Newborn
650	0	4	_aMale
650	0	4	_aMicroscopy, Electron
650	0	4	_aNAD(P)H Dehydrogenase (Quinone) _xdeficiency
650	0	4	_aOrgan Specificity
650	0	4	_aTranscription, Genetic
700	1		_aMousson, B
700	1		_aBeugnot, R
700	1		_aDuborjal, H
700	1		_aFeillet, F
700	1		_aPutet, G
700	1		_aPignot-Paintrand, I
700	1		_aLombès, A
700	1		_aDe Coo, R
700	1		_aSmeets, H
700	1		_aLunardi, J
700	1		_aIssartel, J P
773	0		_tThe Journal of clinical investigation _gvol. 104 _gno. 1 _gp. 83-92
856	4	0	_uhttps://doi.org/10.1172/JCI6184 _zAvailable from publisher's website
999			_c10351991 _d10351991