000			02114 a2200637 4500
005			20250514073128.0
264		0	_c20030924
008			200309s 0 0 eng d
022			_a0002-9297
024	7		_a10.1086/377004 _2doi
040			_aNLM _beng _cNLM
100	1		_aMatsumoto, Naomi
245	0	0	_aMutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation. _h[electronic resource]
260			_bAmerican journal of human genetics _cAug 2003
300			_a233-46 p. _bdigital
500			_aPublication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650	0	4	_aAmino Acid Sequence
650	0	4	_aAnimals
650	0	4	_aCHO Cells
650	0	4	_aCatalase _xmetabolism
650	0	4	_aCell Line
650	0	4	_aCricetinae
650	0	4	_aDNA _xgenetics
650	0	4	_aDNA Mutational Analysis
650	0	4	_aFemale
650	0	4	_aGene Expression
650	0	4	_aGenetic Complementation Test
650	0	4	_aGenotype
650	0	4	_aHumans
650	0	4	_aMembrane Proteins _xdeficiency
650	0	4	_aMice
650	0	4	_aMolecular Sequence Data
650	0	4	_aMutation
650	0	4	_aPeroxisomal Disorders _xclassification
650	0	4	_aPeroxisome-Targeting Signal 1 Receptor
650	0	4	_aPhenotype
650	0	4	_aPregnancy
650	0	4	_aRNA, Messenger _xgenetics
650	0	4	_aReceptors, Cytoplasmic and Nuclear _xmetabolism
650	0	4	_aSequence Homology, Amino Acid
650	0	4	_aTemperature
650	0	4	_aTissue Distribution
650	0	4	_aTransfection
650	0	4	_aZellweger Syndrome _xgenetics
700	1		_aTamura, Shigehiko
700	1		_aFuruki, Satomi
700	1		_aMiyata, Non
700	1		_aMoser, Ann
700	1		_aShimozawa, Nobuyuki
700	1		_aMoser, Hugo W
700	1		_aSuzuki, Yasuyuki
700	1		_aKondo, Naomi
700	1		_aFujiki, Yukio
773	0		_tAmerican journal of human genetics _gvol. 73 _gno. 2 _gp. 233-46
856	4	0	_uhttps://doi.org/10.1086/377004 _zAvailable from publisher's website
999			_c12632455 _d12632455