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{ <http://www.tkuhn.ch/bel2nanopub/RAncN-Xm6G6yFH-mMUrUj0u8sU1CUBQjjne-tHeBvhEyA#_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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