000 01800 a2200577 4500
005 20250513144340.0
264 0 _c19980716
008 199807s 0 0 eng d
022 _a0270-7306
024 7 _a10.1128/MCB.18.7.4324
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aOkumoto, K
245 0 0 _aPEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p.
_h[electronic resource]
260 _bMolecular and cellular biology
_cJul 1998
300 _a4324-36 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aAmino Acid Sequence
650 0 4 _aAnimals
650 0 4 _aBase Sequence
650 0 4 _aCHO Cells
650 0 4 _aCell Line
650 0 4 _aCell Line, Transformed
650 0 4 _aCloning, Molecular
650 0 4 _aCricetinae
650 0 4 _aCytosol
650 0 4 _aDNA, Complementary
650 0 4 _aFibroblasts
650 0 4 _aHumans
650 0 4 _aMembrane Proteins
_xgenetics
650 0 4 _aMicrobodies
_xmetabolism
650 0 4 _aMolecular Sequence Data
650 0 4 _aMutagenesis
650 0 4 _aMutation
650 0 4 _aPeroxisomal Disorders
_xveterinary
650 0 4 _aRats
650 0 4 _aSequence Homology, Amino Acid
650 0 4 _aZellweger Syndrome
_xgenetics
650 0 4 _aZinc Fingers
700 1 _aShimozawa, N
700 1 _aKawai, A
700 1 _aTamura, S
700 1 _aTsukamoto, T
700 1 _aOsumi, T
700 1 _aMoser, H
700 1 _aWanders, R J
700 1 _aSuzuki, Y
700 1 _aKondo, N
700 1 _aFujiki, Y
773 0 _tMolecular and cellular biology
_gvol. 18
_gno. 7
_gp. 4324-36
856 4 0 _uhttps://doi.org/10.1128/MCB.18.7.4324
_zAvailable from publisher's website
999 _c9599143
_d9599143