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{ <http://www.tkuhn.ch/bel2nanopub/RAnl0bhw2I8GQLPWm56_OwQIql5_ncsgM4Jt-_WGmeZiQ#_6> ?p ?o ?g. }
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"
In 1986 we postulated that this disorder might be due to mutations in P450 oxidoreductase (POR), the flavoprotein that donates electron to these and all other microsomal P450 enzymes,
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