000			01518 a2200457 4500
005			20250513204334.0
264		0	_c20000414
008			200004s 0 0 eng d
022			_a1434-5161
024	7		_a10.1007/s100380050014 _2doi
040			_aNLM _beng _cNLM
100	1		_aMakino, M
245	0	0	_aMitochondrial DNA mutations in Leigh syndrome and their phylogenetic implications. _h[electronic resource]
260			_bJournal of human genetics _c2000
300			_a69-75 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't
650	0	4	_aAdenosine Triphosphatases _xgenetics
650	0	4	_aAge of Onset
650	0	4	_aChild
650	0	4	_aChild, Preschool
650	0	4	_aDNA Mutational Analysis
650	0	4	_aDNA, Mitochondrial _xgenetics
650	0	4	_aElectron Transport Complex IV _xgenetics
650	0	4	_aFemale
650	0	4	_aHumans
650	0	4	_aInfant
650	0	4	_aLeigh Disease _xenzymology
650	0	4	_aMale
650	0	4	_aMicroscopy, Electron
650	0	4	_aMuscle, Skeletal _xpathology
650	0	4	_aPhylogeny
650	0	4	_aPoint Mutation
650	0	4	_aPolymerase Chain Reaction
650	0	4	_aPolymorphism, Restriction Fragment Length
650	0	4	_aPyruvate Dehydrogenase Complex _xgenetics
700	1		_aHorai, S
700	1		_aGoto, Y
700	1		_aNonaka, I
773	0		_tJournal of human genetics _gvol. 45 _gno. 2 _gp. 69-75
856	4	0	_uhttps://doi.org/10.1007/s100380050014 _zAvailable from publisher's website
999			_c10675495 _d10675495