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Molecular, biochemical end clinical aspects of peroxisomes biogenesis
disorders
Gootjes, J.
Publication date
2004
Link to publication
Citation for published version (APA):
Gootjes, J. (2004). Molecular, biochemical end clinical aspects of peroxisomes biogenesis
disorders.
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Abbreviations s
AAA A AMACR R BCOX X CG G DBP P DHA A DHAP P DHAPAT T DHCA A FCS S HPLC C IRD D MP P mPTS S NALD D PAGE E PBD D PCR R PEG G PEX X PMP P PP P PTS S PXMP3 3 RCDP P SCOX X SCPx x SDS S THCA A TPR R VLCFA A X-ALD D ZS SATPasee associated with a various cellular activities a-methylacyl-CoAA racemase
brartched-chainn acyl-CoA oxidase complementationn group D-bifuncionall protein docosahexaenoicc acid dihydroxyacetonephosphate e dihydroxyacetonephosphateacyltransferase e dihydroxycholestanoicc acid
fetall calf serum
highh performance liquid chromatography infantilee Refsum disease
matrixx protein
membranee protein peroxisomal targeting signal neonatall adrenoleukodystrophy
polyacrylamidee gel electrophoresis peroxisomee biogenesis disorder polymerasee chain reaction polyethylenee glycol peroxin n
peroxisomall membrane protein pre-peroxisome e
peroxisomall targeting signal
peroxisomall membrane protein 3, PEX2 rhizomelicc chondrodysplasia punctata straight-chainn acyl-CoA oxidase sterol-carrierr protein X
sodiumm dodecyl sulfate trihydroxycholestanoicc acid tetratricopeptidee repeat very-longg chain fatty acid X-linkedd adrenoleukodystrophy Zellwegerr syndrome